FDA Inspection 794296 — SOFIE Co.

SOFIE Co. — FEI 3005705842

The FDA completed an inspection of SOFIE Co. on August 16, 2012 in Morgantown, WV. 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
August 16, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Morgantown, WV (United States)