FDA Inspection 657579 — SunMed AP, Ltd.
The FDA completed an inspection of SunMed AP, Ltd. on March 4, 2010 in Zhuhai. 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
- March 4, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Zhuhai (China)