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FDA Inspection 903219 — Aplicare Products, LLC

Aplicare Products, LLC — FEI 1220701

The FDA completed an inspection of Aplicare Products, LLC on November 17, 2014 in Meriden, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 17, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Meriden, CT (United States)

Facility

Other inspections at this facility

  • 1147759 (OAI Tue Aug 03 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988787 (VAI Fri Sep 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 957238 (OAI Fri Jan 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876204 (NAI Fri Apr 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 797580 (VAI Thu Sep 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources