FDA Inspection 837640 — Hubei Qianjiang Kingphar Medical Material Co. Ltd.
The FDA completed an inspection of Hubei Qianjiang Kingphar Medical Material Co. Ltd. on April 25, 2013 in Qian Jiang. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 25, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Qian Jiang (China)