FDA Inspection 810434 — Phadia US, Inc.

Phadia US, Inc. — FEI 3000214893

The FDA completed an inspection of Phadia US, Inc. on Dec 14, 2012 in Carthage, MO. 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
Dec 14, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Carthage, MO (United States)