FDA Inspection 1076910 — SOFIE Co.

SOFIE Co. — FEI 3008310003

The FDA completed an inspection of SOFIE Co. on January 22, 2019 in Kansas City, MO. 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
January 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)