FDA issued a Warning Letter to Aplicare, Inc. on 12/15/2016 as a result of this inspection.
483 Aplicare Jan 2016

483 Aplicare Jan 2016

Robert Martin FDA, Nealie Newberger FDA$119.00 - Available Now

FDA investigators audited the Aplicare - Meriden, CT, United States facility and issued 6 inspectional observations (via FDA 483) on 15 Jan 2016.

Product details

  • Category: Human Drugs
  • Number of Observations: 6
  • Inspection end: 15 Jan 2016
  • Location: Meriden, United States
  • FEI: 1220701
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