# FDA Inspection 1276832 - ARCHFORM INC - July 28, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/archform-inc/45a55cbe-221e-4e14-a41a-ad02912de6cd
Source feed: FDA_Inspections

> FDA Inspection 1276832 for ARCHFORM INC on July 28, 2025. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276832 - 2025-07-28](https://www.globalkeysolutions.net/records/fda_inspections/archform-inc/eb1d4843-2774-4f09-8338-48589cfb9b12)
- [FDA Inspection 1276832 - 2025-07-28](https://www.globalkeysolutions.net/records/fda_inspections/archform-inc/fede2953-bb29-4023-bf53-fc85eff12f09)
- [FDA Inspection 1276832 - 2025-07-28](https://www.globalkeysolutions.net/records/fda_inspections/archform-inc/9dbbe6a7-d6e9-4f0a-be48-0703246fd0bf)

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

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7