# FDA Inspection 1263279 - Ruhof Corporation - March 07, 2025

Source: https://www.keypedia.com/records/fda_inspections/ruhof-corporation/e4679fea-51f8-417e-89ea-19deca840dae
Source feed: FDA_Inspections

> FDA Inspection 1263279 for Ruhof Corporation on March 07, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263279
- Company Name: Ruhof Corporation
- Inspection Date: 2025-03-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New York District Office

## Related Documents

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Company: https://www.keypedia.com/companies/ruhof-corporation/0c3ccdb6-21d3-4b14-bf04-3841962c3b83

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