FDA Inspection 1040314 — Steribite, LLC
The FDA completed an inspection of Steribite, LLC on December 21, 2017 in Wooster, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 21, 2017
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Wooster, OH (United States)