# Deretil, S.A. – FDA Inspection, Mar 24, 2023

Source: https://www.keypedia.com/records/fda_inspections/deretil-sa/08600e27-fed5-4bd5-a87c-4af60fbb922b
Source feed: FDA_Inspections

> FDA inspection 1203851 of Deretil, S.A., March 24, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1203851
- Company Name: Deretil, S.A.
- Inspection Date: 2023-03-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1132248 - 2019-03-13
- FDA Inspection 956681 - 2016-01-08
- FDA Inspection 850522 - 2013-09-26
- FDA Inspection 674453 - 2010-07-01

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/dennis-cantellops-paite/3336bbb8-8520-4a8a-9085-76e7a55ca773)

Company: https://www.keypedia.com/companies/deretil-sa/39f0d91d-3c36-4439-b6e9-c663ab3bfe7d

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c