FDA Inspection
Sicor S.r.l.Sicor S.r.l. – FDA Inspection, Sep 15, 2017
Record Details
This FDA Inspection record concerns Sicor S.r.l., with an inspection on September 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b74978d7-1e58-4bac-bcb2-d69377080313
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1031160
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Sicor S.r.l.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 15, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 21, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 22, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 12, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 16, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sicor S.r.l.
- FDA Inspection 1215822 - 2022-04-15
- FDA Inspection 1095117 - 2018-12-21
- FDA Inspection 957023 - 2016-01-22
- FDA Inspection 812569 - 2012-12-12
- FDA Inspection 717899 - 2010-12-16
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