FDA Inspection
Olon S.p.A.Olon S.p.A. – FDA Inspection, May 18, 2018
Record Details
This FDA Inspection record concerns Olon S.p.A., with an inspection on May 18, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 2ed0a517-1058-4d24-8b85-be0f155a2a4d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1054684
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Olon S.p.A.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 16, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 24, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 23, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 19, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 19, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Olon S.p.A.
- FDA Inspection 1278287 - 2023-02-16
- FDA Inspection 1129833 - 2020-01-24
- FDA Inspection 1086778 - 2018-03-23
- FDA Inspection 961273 - 2016-02-19
- FDA Inspection 854365 - 2013-09-19
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