FDA Inspection 1002025 — Action-Pak, Inc.

Action-Pak, Inc. — FEI 3002303857

The FDA completed an inspection of Action-Pak, Inc. on Nov 16, 2016 in Camden, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 16, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Camden, NJ (United States)

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