FDA Inspection
McDermott Laboratories Ltd. trading as Mylan Dublin RespiratoryMcDermott Laboratories Ltd. trading as Mylan Dublin Respiratory – FDA Inspection, Jan 19, 2019
Record Details
This FDA Inspection record concerns McDermott Laboratories Ltd. trading as Mylan Dublin Respiratory, with an inspection on January 19, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- January 19, 2019
- Product Type
- Drugs
- Person
- MRA DavisM (Issuing Officer)
View Company Profile
ID · e3b72ebb-0ea5-4c1e-9cfe-9aae6bfb4842
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1112820
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of McDermott Laboratories Ltd. trading as Mylan Dublin Respiratory
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 11, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 1, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for McDermott Laboratories Ltd. trading as Mylan Dublin Respiratory
- FDA Inspection 1267110 - 2022-03-11
- FDA Inspection 983516 - 2016-07-01
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