Traduction de «product inspector » (Anglais → Français) :

(Return tabled) Question No. 452 Mr. Matthew Kellway: With regard to suppliers of garments and textiles that are manufactured outside Canada, in whole or in part, and which have been contracted by any agency or department of the government: (a) what is the process by which Public Works and Government Services Canada (PWGSC) may ask suppliers for evidence of compliance with local labour laws; (b) on how many occasions has PWGSC asked suppliers for evidence of compliance with local labour laws; (c) if PWGSC has ever requested evidence of supplier compliance with local labour laws, (i) which office within PWGSC initiated these requests and under whose authority, (ii) why were these requests initiated, (iii) when were these requests initiated ...[+++], (iv) were these requests for evidence limited in scope to the production process under the direct purview of the supplier, or did they extend to all inputs in the production process even if these inputs were contracted out or otherwise not directly manufactured by the supplier, (v) what type of evidence did PWGSC ask suppliers to provide, (vi) did PWGSC request that suppliers provide evidence verified by independent auditors or inspectors, (vii) did PWGSC ever give individuals from the public, organizations, or governments an opportunity to provide evidence about supplier compliance with local labour laws and to whom were these opportunities extended; (d) if suppliers have ever responded to requests made by the PWGSC for evidence of compliance with local labour laws, (i) how did suppliers respond to these requests, (ii) what information did suppliers provide as evidence, (iii) where and at which office are records of these responses kept, (iv) what method was used by PWGSC to ensure that evidence provided by these suppliers was accurate, (v) did PWGSC ever rely on the services of independent auditors or inspectors to verify the evidence provided by suppliers; (e) what is PWGSC’s policy toward suppliers that are not operating i ...

(Return tabled) Question No. 294 Mr. Frank Valeriote: With respect to the Canadian Food Inspection Agency (CFIA) and its responsibilities for the administration of the food labelling, packaging and advertising policies under the Consumer Packaging and Labelling Act: (a) what is the total number, for each of the fiscal years from 2005-2006 to 2011-2012, across Canada as a whole and broken down by province, of (i) inspectors at the CFIA, (ii) newly hired inspectors at the CFIA, (iii) inspectors who retired from the CFIA, (iv) employees assigned to the CFIA Process, Formulation and Label Registration Unit; (b) what is the total number, for ...[+++] each of the fiscal years from 2005-2006 to 2011-2012, across Canada as a whole and broken down by province, of inspections conducted by a CFIA inspector of a product at a dealer, broken down by (i) retailer, (ii) manufacturer, (iii) processor, (iv) producer, (v) business engaged in importing any product, (vi) business engaged in packing any product, (vii) business engaged in selling any product; (c) for the answer to each part of (b), was the inspection at (i) a site randomly selected, (ii) a site in which the inspection was pre-arranged with any of the individuals or groups identified in (b); (d) for the answer to each part of (c), was the reason for the inspection related to (i) misleading advertising or labelling of exaggerated or unproven nutrition and health claims, (ii) misleading labelling information of the country of origin claims; (e) for the answer to each part of (b), (c) and (d), how many, (i) products or any labelling, packaging or advertising materials were seized and detained by the inspectors, (ii) cases of non-compliance were identified during inspections; (f) for the answer to each part of (e), how many inspections lead to (i) the prosecution of an individual, (ii) the prosecution of a dealer, (iii) a summary conviction or a conviction on indictments of an individual with a fine, (iv) a summary conviction or a ...

Question No. 39 Mr. Francis Scarpaleggia: With regard to water bottled and sold in Canada: (a) how does the government ensure the quality and safety of this food product; (b) does the government regularly send federal inspectors into all water-bottling plants to test bottling processes and product samples and, if so, how many times per year do inspectors visit a given bottling plant and how many inspectors are currently available for plant inspections; (c) how many inspectors were available in February 2005, 2006, 2007 and 2008, res ...[+++]pectively; (d) is a water bottling company required to report to the government the contamination of its product detected by internal testing procedures; (e) is the company required to inform the public and conduct a product recall; (f) how are quality standards for bottled water set in Canada; (g) are standards simply imported from other countries, such as the United States, or are standards developed in Canada for the Canadian market; and (h) what is the relationship between federal bottled-water quality standards and municipal drinking-water standards in Canada?

The undersigned official inspector hereby declares that he/she is aware of the provisions of Decision 96/77/EC and that the attached analytical report(s) correspond(s) to the test carried out in the products after processing.

2. Where, in accordance with Article 122 of Directive 2001/83/EC, the Commission is informed of serious differences of opinion between Member States as to whether the holder of the marketing authorisation for the medicinal product for human use or a manufacturer or importer established within the Community satisfies the requirements referred to in paragraph 1, the Commission may, after consultation with the Member States concerned, request an inspector from the supervisory authority to undertake a new inspection of the marketing autho ...[+++]risation holder, the manufacturer or the importer; the inspector in question shall be accompanied by two inspectors from Member States which are not party to the dispute or by two experts nominated by the Committee for Medicinal Products for Human Use.

2. Where, in accordance with Article 90 of Directive 2001/82/EC, the Commission is informed of serious differences of opinion between Member States as to whether the holder of the marketing authorisation for the veterinary medicinal product or a manufacturer or importer established within the Community satisfies the requirements referred to in paragraph 1, the Commission may, after consultation with the Member States concerned, request an inspector from the supervisory authority to undertake a new inspection of the holder of the marke ...[+++]ting authorisation, the manufacturer or the importer; the inspector in question shall be accompanied by two inspectors from Member States which are not party to the dispute and/or by two experts nominated by the Committee for Medicinal Products for Veterinary Use.