FDA issued a Warning Letter to Aplicare, Inc. on 12/15/2016 for a later inspection.
483 Aplicare Sep 2012

483 Aplicare Sep 2012

Maya Davis FDA$119.00 - Available Now

FDA investigators audited the Aplicare - Meriden, CT, United States facility and issued 5 inspectional observations (via FDA 483) on 06 Sep 2012.

Product details

  • Category: Human Drugs
  • Number of Observations: 5
  • Inspection end: 06 Sep 2012
  • Location: Meriden, United States
  • FEI: 1220701
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