# Ruhof Corporation - Inspection Records

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

> Inspection records and compliance data for Ruhof Corporation in Mineola, New York. Access full analysis and detailed observations.

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## Details

- Name: Ruhof Corporation
- FEI Number: 3003207991
- City: Mineola
- State: New York
- Country Name: United States
- Address Line 1: 393 Sagamore Ave
- Zip Code: 11501

## Related Documents

- [483 - Ruhof Corporation - 2025-03-07](https://www.keypedia.com/records/483/ruhof-corporation/7c7fcd15-ff66-4a4f-a646-0b3a4cd526ea) — source: FDA, date: March 7, 2025
- [FDA Inspection 1263279 - Ruhof Corporation - 2025-03-07](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/15088b2f-ba78-4c01-9d74-7062210adbe6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1263279 - Ruhof Corporation - 2025-03-07](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/e4679fea-51f8-417e-89ea-19deca840dae) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1263279 - Ruhof Corporation - 2025-03-07](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/4a29edaf-3301-446a-896b-680f8f1d6312) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1263279 - Ruhof Corporation - 2025-03-07](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/17d9c2fa-922d-47ff-bf2b-888790fa5e0b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 7, 2025
- [FDA Inspection 1158005 - Ruhof Corporation - 2021-10-28](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/4e855204-6b81-4b6d-999b-3215c79d0fb5) — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2021
- [FDA Inspection 1158005 - Ruhof Corporation - 2021-10-28](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/9bafbe93-2748-4c03-9b1f-3628d6af3ebc) — classification: No Action Indicated (NAI), source: FDA, date: October 28, 2021
- [FDA Inspection 1040052 - Ruhof Corporation - 2017-10-18](https://www.keypedia.com/records/fda_inspections/ruhof-corporation/9c756f3a-7915-4b07-a0b1-f128f5172bb4) — classification: No Action Indicated (NAI), source: FDA, date: October 18, 2017

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