FDA Inspection 904085 — Sterex Electrolysis Int Ltd
The FDA completed an inspection of Sterex Electrolysis Int Ltd on Nov 6, 2014 in Birmingham. 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
- Nov 6, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Birmingham (United Kingdom)