FDA inspection
McDermott Laboratories Ltd. trading as Mylan Dublin Respiratory: FDA inspection ending Jul 1, 2016
FDA inspection 983516 · No Action Indicated (NAI) · Dublin
Key facts
| Inspection ID | 983516 |
|---|---|
| Firm | McDermott Laboratories Ltd. trading as Mylan Dublin Respiratory |
| FEI number | 3011420468 |
| Address | Unit 25 Grange Parade |
| City | Dublin |
| Country | Ireland |
| Fiscal year | 2016 |
| Inspection end date | Jul 1, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data