FDA Inspection 839403 — SOFIE Co.

SOFIE Co. — FEI 3008310003

The FDA completed an inspection of SOFIE Co. on Jul 12, 2013 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 12, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)

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