# ARCHFORM INC – FDA Inspection, Jul 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/archform-inc/fede2953-bb29-4023-bf53-fc85eff12f09
Source feed: FDA_Inspections

> FDA inspection 1276832 of ARCHFORM INC, July 28, 2025. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276832
- Company Name: ARCHFORM INC
- Inspection Date: 2025-07-28
- 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: San Francisco District Office
- Citation Count: 3

## Related Officers

- [Kenya Destin](https://www.keypedia.com/people/kenya-destin/1a367d64-8171-4dfd-bb1f-78d8b96a99f5)
- [Issuing Officer](https://www.keypedia.com/people/kevin-t-le/cf8b5086-f585-4dd5-9f5c-f082b8a340f4)

Company: https://www.keypedia.com/companies/archform-inc/8f988a91-2408-439e-9ead-49dd986f4ba2

Office: https://www.keypedia.com/offices/san-francisco-district-office/6f838e9c-aae1-4665-9c46-a51d43be02df