# FDA Inspection 1291292 - Kerber USA Inc. - November 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/1a881ba1-eea6-4d38-bdfd-948eda69ad81
Source feed: FDA_Inspections

> FDA Inspection 1291292 for Kerber USA Inc. on November 07, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1291292
- Company Name: Kerber USA Inc.
- Inspection Date: 2025-11-07
- 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 1291292 - 2025-11-07](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/ca754e24-7848-42c7-8bd0-e5a92208a12d)
- [FDA Inspection 1291292 - 2025-11-07](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/138a39ce-87d1-4546-9976-dbea19db51e6)
- [FDA Inspection 1291292 - 2025-11-07](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/76364abd-66fc-4003-9145-479c3adff702)
- [FDA Inspection 1187428 - 2022-11-02](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/5d0df877-32ae-455f-acbe-5a93768fbf9a)
- [FDA Inspection 1187428 - 2022-11-02](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/eafe11e1-6719-4004-9965-099449d3a5f0)

Company: https://www.keypedia.com/companies/kerber-usa-inc/299afbad-6c0d-4558-9c3d-2535d4d0c23a

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