Home / Inspections / 784070

FDA Inspection 784070 — Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.

Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. — FEI 3004944662

The FDA completed an inspection of Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd. on May 11, 2012 in Dongyang. 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
May 11, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dongyang (China)

Facility

Other inspections at this facility

  • 1270545 (NAI Fri Apr 11 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1056868 (NAI Fri May 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950773 (VAI Fri Dec 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 882356 (VAI Fri May 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 565677 (NAI Thu Jan 22 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources