FDA Inspection
Delpharm Milano SrlDelpharm Milano Srl – FDA Inspection, May 12, 2017
Record Details
This FDA Inspection record concerns Delpharm Milano Srl, with an inspection on May 12, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- MRA McCulloughJ (Issuing Officer)
View Company Profile
ID · 5408e118-7edc-4718-bef8-27fadf1cac57
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1063879
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Delpharm Milano Srl
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 18, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 25, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 19, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 24, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Delpharm Milano Srl
- FDA Inspection 1175485 - 2022-02-18
- FDA Inspection 948558 - 2015-09-25
- FDA Inspection 857590 - 2013-09-19
- FDA Inspection 740714 - 2011-06-24
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