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

Source: https://www.keypedia.com/records/fda_inspections/ruhof-corporation/17d9c2fa-922d-47ff-bf2b-888790fa5e0b
Source feed: FDA_Inspections

> FDA Inspection 1263279 for Ruhof Corporation on March 07, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263279
- Company Name: Ruhof Corporation
- Inspection Date: 2025-03-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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