FDA Inspection 810182 — Syntermed, Inc.
The FDA completed an inspection of Syntermed, Inc. on Nov 30, 2012 in Atlanta, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 4 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 30, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Atlanta, GA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 14722 | 21 CFR 820.40 | Procedures not adequately established or maintained |
| 3201 | 21 CFR 820.40(a) | Not approved or obsolete document retrieval |
| 3266 | 21 CFR 820.86 | Acceptance status |
| 537 | 21 CFR 820.70(a) | Production processes |