FDA Inspection 992239 — MEDTRONIC IRELAND
The FDA completed an inspection of MEDTRONIC IRELAND on Oct 27, 2016 in Galway. 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
- Oct 27, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Galway (Ireland)