FDA issued a Warning Letter to Lehigh Valley Technologies, Inc. on 7/15/2011 for a previous inspection.
483 Genus Lifesciences Jul 2018

483 Genus Lifesciences Jul 2018

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FDA investigators audited the Genus Lifesciences - Allentown, PA, United States facility and issued inspectional observations (via FDA 483) on 20 Jul 2018.

Product details

  • Category: Human Drugs
  • Inspection end: 20 Jul 2018
  • Location: Allentown, United States
  • FEI: 3003851100
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