FDA Inspection 752181 — Kerma Medical Products, Inc
The FDA completed an inspection of Kerma Medical Products, Inc on November 4, 2011 in Suffolk, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 4, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Suffolk, VA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3201 | 21 CFR 820.40(a) | Not approved or obsolete document retrieval |
| 3696 | 21 CFR 820.100(b) | Documentation |