FDA Inspection
Purolite S.R.L.Purolite S.R.L. – FDA Inspection, Feb 26, 2016
Record Details
This FDA Inspection record concerns Purolite S.R.L., with an inspection on February 26, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Purolite S.R.L.
- Inspection Date
- February 26, 2016
- Product Type
- Drugs
View Company Profile
ID · de4c7a6c-986f-4ab2-84d0-b55083de6b41
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 962029
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Purolite S.R.L.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| October 17, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 14, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 20, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 5, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Purolite S.R.L.
- FDA Inspection 1272741 - 2023-10-17
- FDA Inspection 1132108 - 2018-12-14
- FDA Inspection 851438 - 2013-09-20
- FDA Inspection 570873 - 2009-02-05
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