FDA Inspection 837640 — Hubei Qianjiang Kingphar Medical Material Co. Ltd.
The FDA completed an inspection of Hubei Qianjiang Kingphar Medical Material Co. Ltd. on Apr 25, 2013 in Qian Jiang. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 25, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Qian Jiang (China)