# FDA Inspection 1276546 - Pedicraft, Inc. - July 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/pedicraft-inc/425e8644-39ec-4ebe-b7cd-209c2d0dd654
Source feed: FDA_Inspections

> FDA Inspection 1276546 for Pedicraft, Inc. on July 25, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1276546
- Company Name: Pedicraft, Inc.
- Inspection Date: 2025-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276546 - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/4e12d48e-0eeb-4111-aa1f-a96f6e2d7862)
- [FDA Inspection 1276546 - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/5770caf1-56c6-45ec-bbd5-8ed6109d05d1)
- [FDA Inspection 1276546 - 2025-07-25](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/e88c978a-17fd-4694-b194-d1b04ce4c553)
- [FDA Inspection 1115473 - 2020-01-17](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/6b7e38d7-c322-40e2-ac91-aa8ab12e90a7)
- [FDA Inspection 1115473 - 2020-01-17](https://www.keypedia.com/records/fda_inspections/pedicraft-inc/e386b222-7742-4fa0-bb4e-529aba61298a)

Company: https://www.keypedia.com/companies/pedicraft-inc/348fce14-ecf0-487a-9b55-1d1d07357e2a

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