# FDA Inspection 1123836 - Boiron - September 28, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/boiron/35a813f1-53d6-4d8a-ab6e-bd6a8d49fe68
Source feed: FDA_Inspections

> FDA Inspection 1123836 for Boiron on September 28, 2018. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1123836
- Company Name: Boiron
- Inspection Date: 2018-09-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1277384 - 2023-09-15](https://www.globalkeysolutions.net/records/fda_inspections/boiron/c8e4f634-c2ab-4238-9f6d-0166862a460d)
- [FDA Inspection 1017861 - 2017-07-07](https://www.globalkeysolutions.net/records/fda_inspections/boiron/cc619ba0-ee60-4ad7-89ae-a08f3939e4a2)
- [FDA Inspection 912250 - 2015-01-15](https://www.globalkeysolutions.net/records/fda_inspections/boiron/01522329-0af4-4938-b4a1-81349a971451)

Company: https://www.globalkeysolutions.net/companies/boiron/b94ce33e-d525-4346-8542-cd15a3d569bc

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