FDA issued a Warning Letter to Keystone Laboratories Inc on 3/18/2013 for a previous inspection.
483 Keystone Labs Aug 2013

483 Keystone Labs Aug 2013

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FDA investigators audited the Keystone Labs - Memphis, TN, United States facility and issued 10 inspectional observations (via FDA 483) on 15 Aug 2013.

Product details

  • Category: Human Drugs
  • Number of Observations: 10
  • Inspection end: 15 Aug 2013
  • Location: Memphis, United States
  • FEI: 1020139
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