FDA Inspection
Laboratoires DelonLaboratoires Delon – FDA Inspection, Jan 24, 2020
Record Details
This FDA Inspection record concerns Laboratoires Delon, with an inspection on January 24, 2020, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Laboratoires Delon
- Inspection Date
- January 24, 2020
- Product Type
- Drugs
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ID · b28a8ba6-d2fd-4afa-9bc8-3b7a017e1195
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1116000
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.142(b)Storage under appropriate conditions
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Laboratoires Delon
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2025 | VAI | Office of Inspections and Investigations | Drug Quality Assurance |
| December 9, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 7, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Laboratoires Delon
- FDA Inspection 1262809 - 2025-02-21
- FDA Inspection 997025 - 2016-12-09
- FDA Inspection 906587 - 2014-11-07
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