# FDA Inspection 988195 - Konica Minolta Technoproducts Co., Ltd. - February 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/konica-minolta-technoproducts-co-ltd/1f1a68b7-4ec2-468a-ab0b-5f2f0567206c
Source feed: FDA_Inspections

> FDA Inspection 988195 for Konica Minolta Technoproducts Co., Ltd. on February 19, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988195
- Company Name: Konica Minolta Technoproducts Co., Ltd.
- Inspection Date: 2016-02-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988195 - 2016-02-19](https://www.keypedia.com/records/fda_inspections/konica-minolta-technoproducts-co-ltd/240e5b94-4b71-4335-97aa-db74bc2deb17)

Company: https://www.keypedia.com/companies/konica-minolta-technoproducts-co-ltd/d376d282-3561-42c9-b260-7db17341dac1

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