FDA Inspection 834494 — PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD.
The FDA completed an inspection of PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD. on May 16, 2013 in Changzhou. 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
- May 16, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Changzhou (China)