FDA Inspection
Laboratoires DelonLaboratoires Delon – FDA Inspection, Dec 9, 2016
Record Details
This FDA Inspection record concerns Laboratoires Delon, with an inspection on December 9, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b980b906-74e6-4e96-828c-ec210fea3ace
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 997025
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.170(b)Annual visual exams of drug products
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Laboratoires Delon
3| Date | Classification | Office | Project area |
|---|---|---|---|
| February 21, 2025 | VAI | Office of Inspections and Investigations | Drug Quality Assurance |
| January 24, 2020 | 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 1116000 - 2020-01-24
- FDA Inspection 906587 - 2014-11-07
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