FDA Inspection 945810 — PediFix, Inc.

PediFix, Inc. — FEI 3009710062

The FDA completed an inspection of PediFix, Inc. on Oct 13, 2015 in Brewster, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 13, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brewster, NY (United States)

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