# FDA Inspection 1279932 - Trident Manufacturing, Inc. - August 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/trident-manufacturing-inc/17789366-01e4-413c-b718-e40f80ab3d58
Source feed: FDA_Inspections

> FDA Inspection 1279932 for Trident Manufacturing, Inc. on August 28, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1279932
- Company Name: Trident Manufacturing, Inc.
- Inspection Date: 2025-08-28
- 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 1279932 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/trident-manufacturing-inc/8b5a0003-a890-4f1e-b4cb-68f88ee4b21c)
- [FDA Inspection 1279932 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/trident-manufacturing-inc/32c6e84c-0da5-4aa9-8f3f-a0b64f09fcef)
- [FDA Inspection 1279932 - 2025-08-28](https://www.keypedia.com/records/fda_inspections/trident-manufacturing-inc/be460aa9-ef66-4461-93ab-702fb7ee9b36)

Company: https://www.keypedia.com/companies/trident-manufacturing-inc/ca7a94c3-03e9-4365-b6dd-44a4a624ed20

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