FDA Inspection 675641 — Steritec Products Mfg. Co., Inc.
The FDA completed an inspection of Steritec Products Mfg. Co., Inc. on Aug 12, 2010 in Englewood, CO. 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
- Aug 12, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Englewood, CO (United States)