# FDA Inspection 1289318 - Supreme Screw Products - October 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 for Supreme Screw Products on October 29, 2025. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New York District Office

## Related Documents

- [FDA Inspection 1289318 - 2025-10-29](https://www.keypedia.com/records/fda_inspections/supreme-screw-products/d90b1965-56bd-4baa-90b1-5809c5876a97)
- [FDA Inspection 1220480 - 2023-09-06](https://www.keypedia.com/records/fda_inspections/supreme-screw-products/e859a3df-b32b-491a-b85a-a6adfa69697e)
- [FDA Inspection 1220480 - 2023-09-06](https://www.keypedia.com/records/fda_inspections/supreme-screw-products/07dbccf0-3d42-4a8b-aa81-8d75b56c69f7)

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