FDA Inspection 934935 — Digitimer Ltd.
The FDA completed an inspection of Digitimer Ltd. on Jul 2, 2015 in Welwyn Garden City. 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
- Jul 2, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Welwyn Garden City (United Kingdom)