# Konica Minolta Healthcare, Americas, Inc. – FDA Inspection, Aug 25, 2017

Source: https://www.keypedia.com/records/fda_inspections/konica-minolta-healthcare-americas-inc/e08b485d-590f-477b-8038-9344ab7fb8f0
Source feed: FDA_Inspections

> FDA inspection 1022872 of Konica Minolta Healthcare, Americas, Inc., August 25, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022872
- Company Name: Konica Minolta Healthcare, Americas, Inc.
- Inspection Date: 2017-08-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 897362 - 2014-08-20

## Related Officers

- [Company Rep](https://www.keypedia.com/people/samuel-l-murray/74b03eba-03ee-409b-9394-8e903adf6288)

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