FDA Inspection 1280383 — SOFIE Co.

SOFIE Co. — FEI 3008310003

The FDA completed an inspection of SOFIE Co. on September 3, 2025 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 3, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)

Citations

IDCFRDescription
1781221 CFR 212.50Adequate controls (general)