FDA issued a Warning Letter to Aplicare, Inc. on 12/15/2016 for a later inspection.
483 Aplicare Apr 2001

483 Aplicare Apr 2001

Edward Janik FDA, Stephen Souza FDA$119.00 - Available Now

FDA investigators audited the Aplicare - Meriden, CT, United States facility and issued inspectional observations (via FDA 483) on 26 Apr 2001.

Product details

  • Category: Human Drugs / Medical Devices & Rad Health
  • Inspection end: 26 Apr 2001
  • Location: Meriden, United States
  • FEI: 1220701
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