FDA Inspection
Intercos Europe SpAIntercos Europe SpA – FDA Inspection, Jun 24, 2016
Record Details
This FDA Inspection record concerns Intercos Europe SpA, with an inspection on June 24, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Intercos Europe SpA
- Inspection Date
- June 24, 2016
- Product Type
- Drugs
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ID · 19a275e6-3f46-4c9d-856f-047773743fc4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 978093
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.100(a)Absence of Written Procedures
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Other FDA inspections of Intercos Europe SpA
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 29, 2024 | VAI | Office of Inspections and Investigations | Drug Quality Assurance |
| September 11, 2019 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Intercos Europe SpA
- FDA Inspection 1256045 - 2024-11-29
- FDA Inspection 1110083 - 2019-09-11
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