FDA Inspection 992391 — PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD.
The FDA completed an inspection of PARAGON MEDICAL DEVICE (CHANGZHOU) CO., LTD. on October 27, 2016 in Changzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 27, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Changzhou (China)