FDA Inspection
Laboratorios Liomont, S.A. de C.V.Laboratorios Liomont, S.A. de C.V. – FDA Inspection, Aug 4, 2023
Record Details
This FDA Inspection record concerns Laboratorios Liomont, S.A. de C.V., with an inspection on August 4, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 448b720d-a02e-4a81-b7fd-935a431c7804
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1219483
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Laboratorios Liomont, S.A. de C.V.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 15, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 19, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Laboratorios Liomont, S.A. de C.V.
- FDA Inspection 1037943 - 2017-12-15
- FDA Inspection 808251 - 2012-10-19
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