FDA Inspection 915094 — STERIS Corporation
The FDA completed an inspection of STERIS Corporation on February 27, 2015 in Saint Louis, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 27, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Saint Louis, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1207 | 21 CFR 211.65(b) | Substances That Come in Contact |
| 1361 | 21 CFR 211.100(a) | Absence of Written Procedures |
| 3565 | 21 CFR 211.58 | Buildings not maintained in good state of repair |