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The Food and Drug Administration (FDA) has for many years recognized the role of private testing laboratories in determining the quality of foodstuffs imported into the United States. Programs such as automatic detentions ("blocklisting") have resulted in the expanded use of private laboratories by importers. FDA believes that, given agency resource limitations and increasing import obligations, they are obligated to rely to a significant degree on data generated by private laboratories to make compliance decisions. Certified Laboratories, Inc. has been in the forefront among laboratories in dealing with the Food and Drug Administration and working with their programs, not only on automatic detentions but other matters such as referee samples and reconditioning proposals as well.

Because we provide our results to many of the FDA districts throughout the United States we have developed uniform and effective laboratory reporting formats that are uniformly accepted by the agency.

The role of private laboratories and their use by importers is outlined in the Regulatory Procedures Manual (X9-52-1). We at Certified Laboratories, Inc. adhere to those guidelines as well as to all good laboratory practices. For your information we have provided an overview of some of the requirements and procedures that we follow to assure rapid review and acceptance of our reports by FDA Districts.
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