# Kerber USA Inc. – FDA Inspection, Nov 7, 2025

Source: https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/ca754e24-7848-42c7-8bd0-e5a92208a12d
Source feed: FDA_Inspections

> FDA inspection 1291292 of Kerber USA Inc., November 07, 2025. Classification: No Action Indicated (NAI). 10 citations under 21 CFR parts 820 and 830. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1291292
- Company Name: Kerber USA Inc.
- Inspection Date: 2025-11-07
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New York District Office
- Citation Count: 10

## Related Documents

- [FDA Inspection 1187428 - 2022-11-02](https://www.keypedia.com/records/fda_inspections/kerber-usa-inc/eafe11e1-6719-4004-9965-099449d3a5f0)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

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

Office: https://www.keypedia.com/offices/new-york-district-office/9fa3d265-16ca-438d-8a6e-b47f60dc260d