# FDA Inspection 838056 - Konica Minolta, Inc. - May 30, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/konica-minolta-inc/dc9a1e33-e4f6-492c-ad3a-b0b1210c0e51
Source feed: FDA_Inspections

> FDA Inspection 838056 for Konica Minolta, Inc. on May 30, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838056
- Company Name: Konica Minolta, Inc.
- Inspection Date: 2013-05-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838056 - 2013-05-30](https://www.globalkeysolutions.net/records/fda_inspections/konica-minolta-inc/c9545363-c9ca-47f3-acc0-573c247b7b38)

Company: https://www.globalkeysolutions.net/companies/konica-minolta-inc/e6523af2-d06f-4c4e-9ece-7a9dd4cc181a

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