# FDA Inspection 1176638 - Lonza Bend Inc - August 05, 2022

Source: https://www.keypedia.com/records/fda_inspections/lonza-bend-inc/463e45ca-1447-481b-80b6-e0b7b301fb83
Source feed: FDA_Inspections

> FDA Inspection 1176638 for Lonza Bend Inc on August 05, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1176638
- Company Name: Lonza Bend Inc
- Inspection Date: 2022-08-05
- 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 1016970 - 2017-06-30](https://www.keypedia.com/records/fda_inspections/lonza-bend-inc/78836ec5-5699-4203-bd2b-19d1cfd114d2)
- [FDA Inspection 985218 - 2016-06-03](https://www.keypedia.com/records/fda_inspections/lonza-bend-inc/1ff195ed-dca3-457a-81b6-bf7491e00f00)

Company: https://www.keypedia.com/companies/lonza-bend-inc/d574a9e5-f048-4951-89b0-a789d938c962

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