FDA Inspection 1010928 — STERITECH, INC.
The FDA completed an inspection of STERITECH, INC. on Apr 26, 2017 in Salinas, PR. 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
- Apr 26, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Salinas, PR (United States)