FDA Inspection 924881 — Fagron, Inc

Fagron, Inc — FEI 1000174332

The FDA completed an inspection of Fagron, Inc on Apr 29, 2015 in Saint Paul, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 29, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Paul, MN (United States)

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