FDA Inspection 977923 — SOFIE Co.

SOFIE Co. — FEI 3003932395

The FDA completed an inspection of SOFIE Co. on May 6, 2016 in Houston, TX. 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
May 6, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Houston, TX (United States)