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News | August 17, 2013

PBL Successfully Completes FDA GLP Inspection

by PBL

During the week of August 5-9, 2013, the FDA visited Pacific BioLabs to conduct a GLP inspection and audit of the facility in Hercules, CA.

PBL is pleased to report that the inspection did not generate any Form 483 letters or warnings.

This is the eighth consecutive FDA audit PBL has successfully completed without the issuance of a 483, and we are happy to be able to continue to provide the highest level of quality and service to our clients.

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