# GH Genhelix S.A. – FDA Inspection, Dec 12, 2019

Source: https://www.keypedia.com/records/fda_inspections/gh-genhelix-sa/cc7e9e5c-8eef-4b25-8d70-9aad3e0084b8
Source feed: FDA_Inspections

> FDA inspection 1202723 of GH Genhelix S.A., December 12, 2019. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1202723
- Company Name: GH Genhelix S.A.
- Inspection Date: 2019-12-12
- 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 1276827 - 2022-10-26](https://www.keypedia.com/records/fda_inspections/gh-genhelix-sa/f8996d6d-2d43-4287-9114-7e825c8b9cf1)

Company: https://www.keypedia.com/companies/gh-genhelix-sa/510145e8-eb5a-49de-9a89-3cdc1164f0db

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