# Supreme Screw Products – FDA Inspection, Oct 29, 2025

Source: https://www.keypedia.com/records/fda_inspections/supreme-screw-products/ea307c6d-d1d5-41e7-a7fd-a25ca97b07af
Source feed: FDA_Inspections

> FDA inspection 1289318 of Supreme Screw Products, October 29, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289318
- Company Name: Supreme Screw Products
- Inspection Date: 2025-10-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New York District Office
- Citation Count: 3

## Related Documents

- FDA Inspection 1220480 - 2023-09-06

## Related Officers

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

Company: https://www.keypedia.com/companies/supreme-screw-products/ae59279b-ddc7-4f97-8e1f-5d52c79866b0

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