# FDA Inspection 1280300 - GUERBET LLC - August 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/guerbet-llc/2a1fe9f5-32da-4590-a6ad-3c7c9bff260c
Source feed: FDA_Inspections

> FDA Inspection 1280300 for GUERBET LLC on August 28, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280300
- Company Name: GUERBET LLC
- Inspection Date: 2025-08-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarketing Surveillance and Epidemiology: Human Drugs
- Product Type: Human Drugs
- Office Name: New Jersey District Office

## Related Documents

- [FDA Inspection 1280300 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/guerbet-llc/fede157a-0280-4ac6-b9be-19e65434110f)
- [FDA Inspection 918246 - 2015-02-13](https://www.keypedia.com/records/fda_inspections/guerbet-llc/086c1532-7ed5-4309-9ced-b5bc35e30549)
- [FDA Inspection 815122 - 2013-01-14](https://www.keypedia.com/records/fda_inspections/guerbet-llc/c1d57589-b228-409a-95c0-cb0899e7c24e)

Company: https://www.keypedia.com/companies/guerbet-llc/415cb194-2519-4a28-82b2-e5d8846487d0

Office: https://www.keypedia.com/offices/new-jersey-district-office/6ff5e2e9-5cff-44c7-af24-5a55329a8248