FDA Inspection 881951 — Huiheng Medical
The FDA completed an inspection of Huiheng Medical on Jan 27, 2014 in Baton Rouge, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 27, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Baton Rouge, LA (United States)