# FDA Inspection 897362 - Konica Minolta Healthcare, Americas, Inc. - August 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/konica-minolta-healthcare-americas-inc/5ad8686a-cdb3-4d5a-8fd3-386eb513a031
Source feed: FDA_Inspections

> FDA Inspection 897362 for Konica Minolta Healthcare, Americas, Inc. on August 20, 2014. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 897362
- Company Name: Konica Minolta Healthcare, Americas, Inc.
- Inspection Date: 2014-08-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1022872 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/konica-minolta-healthcare-americas-inc/e08b485d-590f-477b-8038-9344ab7fb8f0)
- [FDA Inspection 1022872 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/konica-minolta-healthcare-americas-inc/37a1dac9-6206-4f1c-a2b7-42f91444b629)
- [FDA Inspection 1022872 - 2017-08-25](https://www.keypedia.com/records/fda_inspections/konica-minolta-healthcare-americas-inc/1f3cdda4-3812-4367-b7c2-a17368466878)

Company: https://www.keypedia.com/companies/konica-minolta-healthcare-americas-inc/29f0ab36-f07d-4389-a4b0-6b112712e14b

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