# FDA 483 - Ruhof Corporation - March 07, 2025

Source: https://www.keypedia.com/records/483/ruhof-corporation/7c7fcd15-ff66-4a4f-a646-0b3a4cd526ea

> FDA 483 for Ruhof Corporation on March 07, 2025. Product: other. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Ruhof Corporation
- Inspection Date: 2025-03-07
- Product Type: other
- Office Name: New York District Office
- Summary: Ruhof Corporation, an importer and own label distributor in Mineola, NY, was inspected by the FDA. The inspection revealed a significant issue with the firm's complaint investigation records. Specifically, investigations into allergic reactions involving an endoscopic bite block were found to be incomplete, lacking crucial information about product materials and allergen testing.

## Related Officers

- [Jacqueline S. Warner](https://www.keypedia.com/people/jacqueline-s-warner/d001f4ec-db46-4d78-a5dd-efea7ddfb893)

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