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483 BioReliance, Jul 2012

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by Rachel Harrington FDA

FDA investigators audited the BioReliance - Rockville , MD, United States facility and issued 4 inspectional observations (via FDA 483) on 03 Jul 2012.

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Product Details

  • Category: Animal Drugs & Feeds / Human Drugs
  • Number of Observations: 4
  • Inspection end: 03 Jul 2012
  • Location: Rockville, United States
  • FEI: 1122041
BioReliance FDA inspection 483 Jul 2012

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