# FDA Inspection 1283582 - Armbrust Inc. - September 25, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/armbrust-inc/52352959-5a70-49bd-af0b-b2ea6b911964
Source feed: FDA_Inspections

> FDA Inspection 1283582 for Armbrust Inc. on September 25, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283582
- Company Name: Armbrust Inc.
- Inspection Date: 2025-09-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1283582 - 2025-09-25](https://www.globalkeysolutions.net/records/fda_inspections/armbrust-inc/f4e2139d-a9ed-4618-83ac-9fdf1accdc9f)
- [FDA Inspection 1283582 - 2025-09-25](https://www.globalkeysolutions.net/records/fda_inspections/armbrust-inc/faa9461c-9bb8-4f71-8cc5-90c3af7d25d2)
- [FDA Inspection 1283582 - 2025-09-25](https://www.globalkeysolutions.net/records/fda_inspections/armbrust-inc/2f49a8f6-b119-4df6-a93f-441c5a6ecc47)

Company: https://www.globalkeysolutions.net/companies/armbrust-inc/f263766f-e1aa-4c00-a45b-dec742bf1567

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7