# FDA Inspection 1270251 - Uramix Inc - May 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/uramix-inc/1b6c88df-2011-4bc4-9317-72d5ae6bcd83
Source feed: FDA_Inspections

> FDA Inspection 1270251 for Uramix Inc on May 20, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1270251
- Company Name: Uramix Inc
- Inspection Date: 2025-05-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Philadelphia District Office

## Related Documents

- [FDA Inspection 1270251 - 2025-05-20](https://www.keypedia.com/records/fda_inspections/uramix-inc/31f6c664-cdf3-4f70-9c82-38582f1f8baa)

Company: https://www.keypedia.com/companies/uramix-inc/55166b8b-c674-44f1-91f2-8c3aadf9857d

Office: https://www.keypedia.com/offices/philadelphia-district-office/c5ec7398-b3d5-4125-9793-fb7b972578d8