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483 BioReliance, Feb 2009

$119 - Available for instant download
by Daniel Azar FDA, Ernest Bizjak FDA, Lakisha Williams FDA

FDA investigators audited the BioReliance - Rockville , MD, United States facility and issued inspectional observations (via FDA 483) on 18 Feb 2009.

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Product Details

  • Category: Human Drugs / Biologics
  • Inspection end: 18 Feb 2009
  • Location: Rockville, United States
  • FEI: 1122041
BioReliance FDA inspection 483 Feb 2009

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