# Ruhof Corporation – FDA Inspection, Oct 28, 2021

Source: https://www.keypedia.com/records/fda_inspections/ruhof-corporation/9bafbe93-2748-4c03-9b1f-3628d6af3ebc
Source feed: FDA_Inspections

> FDA inspection 1158005 of Ruhof Corporation, October 28, 2021. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1158005
- Company Name: Ruhof Corporation
- Inspection Date: 2021-10-28
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1263279 - 2025-03-07](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/e4679fea-51f8-417e-89ea-19deca840dae)
- FDA Inspection 1040052 - 2017-10-18

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