FDA Inspection 1003248 — Primus Sterilizer Co Inc
The FDA completed an inspection of Primus Sterilizer Co Inc on Feb 21, 2017 in Great Bend, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 21, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Great Bend, KS (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 |