FDA Inspection 970671 — SOFIE Co.

SOFIE Co. — FEI 3008486071

The FDA completed an inspection of SOFIE Co. on May 27, 2016 in Dallas, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 27, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dallas, TX (United States)

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