# FDA Inspection 1202192 - Konica Minolta, Inc. - April 05, 2023

Source: https://www.keypedia.com/records/fda_inspections/konica-minolta-inc/ac814854-9ab5-48cf-ad46-c1df275d8f59
Source feed: FDA_Inspections

> FDA Inspection 1202192 for Konica Minolta, Inc. on April 05, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202192
- Company Name: Konica Minolta, Inc.
- Inspection Date: 2023-04-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1202192 - 2023-04-05](https://www.keypedia.com/records/fda_inspections/konica-minolta-inc/821756d2-5a02-48ac-b481-bb4759157d3a)

Company: https://www.keypedia.com/companies/konica-minolta-inc/b76ca4db-ca56-41e7-bdf6-1841b545d2e9

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