# Lonza AG – FDA Inspection, Dec 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/lonza-ag/6aabdbe9-cb78-4447-878b-509514b56a44
Source feed: FDA_Inspections

> FDA inspection 1035618 of Lonza AG, December 15, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 11 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1035618
- Company Name: Lonza AG
- Inspection Date: 2017-12-15
- 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

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## Related Officers

- Issuing Officer
- [Issuing Officer](https://www.keypedia.com/people/frances-namuswe/d64cc7a2-3840-41c9-ae6c-fe225a651369)
- Issuing Officer
- [Issuing Officer](https://www.keypedia.com/people/tiara-n-brown-crosen/8255649d-25a9-49fa-a28d-0cdda922c0c3)

Company: https://www.keypedia.com/companies/lonza-ag/7084f7e6-ce36-429f-942a-28e759416e70

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