FDA Inspection 914385 — Primus Sterilizer Co Inc
The FDA completed an inspection of Primus Sterilizer Co Inc on Jan 28, 2015 in Great Bend, KS. 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 28, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Great Bend, KS (United States)