# FDA Inspection 988196 - Konica Minolta Technoproducts Co., Ltd. - February 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/konica-minolta-technoproducts-co-ltd/95d0feea-dda1-4419-a97f-c49c9def7990
Source feed: FDA_Inspections

> FDA Inspection 988196 for Konica Minolta Technoproducts Co., Ltd. on February 23, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 988196
- Company Name: Konica Minolta Technoproducts Co., Ltd.
- Inspection Date: 2016-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 988196 - 2016-02-23](https://www.keypedia.com/records/fda_inspections/konica-minolta-technoproducts-co-ltd/38bca907-5c4d-4412-9b75-fba0a49ec9c3)

Company: https://www.keypedia.com/companies/konica-minolta-technoproducts-co-ltd/5ddf0ec0-5c4f-4d20-aa90-355374bac43f

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