FDA Inspection 977039 — Kapitex Healthcare Ltd
The FDA completed an inspection of Kapitex Healthcare Ltd on Feb 10, 2016 in Wetherby. 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
- Feb 10, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Wetherby (United Kingdom)