FDA Inspection 834493 — Primus Sterilizer Co Inc
The FDA completed an inspection of Primus Sterilizer Co Inc on May 10, 2013 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
- May 10, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Great Bend, KS (United States)