FDA Inspection 904708 — MEDTRONIC IRELAND
The FDA completed an inspection of MEDTRONIC IRELAND on November 20, 2014 in Galway. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 20, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Galway (Ireland)
Additional Details
Postmarket Audit Inspections