# FDA Inspection 1287220 - Edmundowicz, Dr Steven - October 09, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/edmundowicz-dr-steven/df37a300-4bf2-4cd3-8246-8e23c1f538fa
Source feed: FDA_Inspections

> FDA Inspection 1287220 for Edmundowicz, Dr Steven on October 09, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1287220
- Company Name: Edmundowicz, Dr Steven
- Inspection Date: 2025-10-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Denver District Office

## Related Documents

- [FDA Inspection 1287220 - 2025-10-09](https://www.globalkeysolutions.net/records/fda_inspections/edmundowicz-dr-steven/5a188ab6-9426-4c78-8ed1-9f3168d4b11a)
- [FDA Inspection 900972 - 2014-10-14](https://www.globalkeysolutions.net/records/fda_inspections/edmundowicz-dr-steven/e1d55367-b135-4abf-bb3e-4679203cad6d)

Company: https://www.globalkeysolutions.net/companies/edmundowicz-dr-steven/8790bc54-e3c6-4165-a1d4-a6b67c236dc6

Office: https://www.globalkeysolutions.net/offices/denver-district-office/93b79063-390c-4759-af6c-5da7e388face