FDA Inspection 589589 — Alwyn Co., Inc.

Alwyn Co., Inc. — FEI 1000520217

The FDA completed an inspection of Alwyn Co., Inc. on June 12, 2009 in Eagan, 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
June 12, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Eagan, MN (United States)