# FDA Inspection 887240 - Ajinomoto Omnichem - June 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/ajinomoto-omnichem/ca8f93f1-3ada-45f1-bd14-cad6bba2b1ef
Source feed: FDA_Inspections

> FDA Inspection 887240 for Ajinomoto Omnichem on June 20, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 887240
- Company Name: Ajinomoto Omnichem
- Inspection Date: 2014-06-20
- 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 1207801 - 2022-12-16](https://www.keypedia.com/records/fda_inspections/ajinomoto-omnichem/67e35dde-3d26-4437-b512-e15a08c70b39)
- [FDA Inspection 1057668 - 2018-06-29](https://www.keypedia.com/records/fda_inspections/ajinomoto-omnichem/36f57573-6ec0-4640-8f0f-7c9635085021)
- [FDA Inspection 755921 - 2011-11-10](https://www.keypedia.com/records/fda_inspections/ajinomoto-omnichem/72bab479-b2e0-4c57-9d87-c750366269bf)

Company: https://www.keypedia.com/companies/ajinomoto-omnichem/1c295d35-5beb-4f6c-9f60-ccc3d2ce2b1a

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