FDA Inspection 793088 — Fagron, Inc

Fagron, Inc — FEI 1000174332

The FDA completed an inspection of Fagron, Inc on July 27, 2012 in Saint Paul, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 27, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Paul, MN (United States)