# PHEN"X TECHNOLOGIES – FDA Inspection, Jun 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/phenx-technologies/c94df6f3-0ef1-47d5-9c23-d0a1a30b9e6f
Source feed: FDA_Inspections

> FDA inspection 1276579 of PHEN"X TECHNOLOGIES, June 26, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276579
- Company Name: PHEN"X TECHNOLOGIES
- Inspection Date: 2025-06-26
- 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: Office of Inspections and Investigations
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/albert-l-nguyen/496338d0-71c4-43da-92f0-09515559d9fc)

Company: https://www.keypedia.com/companies/phenx-technologies/2af65ac3-4dca-468f-9ed1-82a208501505

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8
