FDA Inspection 987872 — Hubei Yitai Pharmaceutical Co., Ltd

Hubei Yitai Pharmaceutical Co., Ltd — FEI 3004844161

The FDA completed an inspection of Hubei Yitai Pharmaceutical Co., Ltd on Sep 22, 2016 in Tianmen. 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
Sep 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tianmen (China)

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