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FDA Inspection 607549 — Aplicare Products, LLC

Aplicare Products, LLC — FEI 1220701

The FDA completed an inspection of Aplicare Products, LLC on August 7, 2009 in Meriden, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 7, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Meriden, CT (United States)

Facility

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FDA data resources