FDA Inspection 636425 — Aplicare Products, LLC

Aplicare Products, LLC — FEI 1220701

The FDA completed an inspection of Aplicare Products, LLC on December 17, 2009 in Meriden, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 17, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Meriden, CT (United States)

Citations

IDCFRDescription
202821 CFR 211.192Extent of discrepancy, failure investigations