# FDA Inspection 1279128 - Brighton Laboratory - August 21, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/brighton-laboratory/be28a98c-c7bd-45fc-9b3a-6aa12381ec9e
Source feed: FDA_Inspections

> FDA Inspection 1279128 for Brighton Laboratory on August 21, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279128
- Company Name: Brighton Laboratory
- Inspection Date: 2025-08-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Human Drugs
- Office Name: San Francisco District Office

## Related Documents

- [FDA Inspection 1055645 - 2018-05-15](https://www.globalkeysolutions.net/records/fda_inspections/brighton-laboratory/559627f8-f512-4aa6-8edd-52d939784905)

Company: https://www.globalkeysolutions.net/companies/brighton-laboratory/7b9543dc-6111-4408-be79-4086d1309969

Office: https://www.globalkeysolutions.net/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df