FDA Inspection 588900 — Syntec Inc
The FDA completed an inspection of Syntec Inc on Jun 12, 2009 in Winfield, MO. 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
- Jun 12, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Winfield, MO (United States)