# FDA Inspection 1206900 - Asahi Intecc Usa Inc - June 01, 2023

Source: https://www.keypedia.com/records/fda_inspections/asahi-intecc-usa-inc/d4cdbb99-64ed-48f7-baba-4f12287450e1
Source feed: FDA_Inspections

> FDA Inspection 1206900 for Asahi Intecc Usa Inc on June 01, 2023. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1206900
- Company Name: Asahi Intecc Usa Inc
- Inspection Date: 2023-06-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1206900 - 2023-06-01](https://www.keypedia.com/records/fda_inspections/asahi-intecc-usa-inc/2fa108b3-fc04-4937-a7e6-5c61d8f46194)
- [FDA Inspection 671227 - 2010-06-29](https://www.keypedia.com/records/fda_inspections/asahi-intecc-usa-inc/61688329-5ecd-4f3c-96ab-9e7bf030776b)
- [FDA Inspection 671227 - 2010-06-29](https://www.keypedia.com/records/fda_inspections/asahi-intecc-usa-inc/303b90fd-22a9-46c3-87f8-7b32c5d27849)

Company: https://www.keypedia.com/companies/asahi-intecc-usa-inc/62d9e9d8-6d0d-4162-aa71-9ea5bb630c55

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