FDA Inspection 983516 — McDermott Laboratories Ltd. Trading As Mylan Dublin Respiratory
The FDA completed an inspection of McDermott Laboratories Ltd. Trading As Mylan Dublin Respiratory on Jul 1, 2016 in Dublin. 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 1, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Dublin (Ireland)