FDA Inspection
Intercos Europe S.p.AIntercos Europe S.p.A – FDA Inspection, Feb 13, 2015
Record Details
This FDA Inspection record concerns Intercos Europe S.p.A, with an inspection on February 13, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Intercos Europe S.p.A
- Inspection Date
- February 13, 2015
- Product Type
- Drugs
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ID · 75d48cde-0c39-497a-9ed1-89f05fc4268c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 922885
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Intercos Europe S.p.A
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 15, 2024 | OAI | Office of Inspections and Investigations | Drug Quality Assurance |
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