FDA Inspection 636425 — Aplicare Products, LLC

Aplicare Products, LLC — FEI 1220701

The FDA completed an inspection of Aplicare Products, LLC on Dec 17, 2009 in Meriden, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 17, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Meriden, CT (United States)

Citations

IDCFRDescription
202821 CFR 211.192Extent of discrepancy, failure investigations

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