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FDA Inspection 1021133 — Zhejiang Medicine Co. Ltd. Xinchang Pharmaceutical Factory

Zhejiang Medicine Co. Ltd. Xinchang Pharmaceutical Factory — FEI 3003631275

The FDA completed an inspection of Zhejiang Medicine Co. Ltd. Xinchang Pharmaceutical Factory on June 30, 2017 in Xinchang. 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
June 30, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Xinchang (China)

Facility

Other inspections at this facility

  • 1265665 (VAI Fri Mar 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1076284 (VAI Fri Nov 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 936929 (OAI Thu Jun 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 818048 (NAI Thu Jan 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 682116 (VAI Fri Apr 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources