# FDA Inspection 989174 - Nipro Diagnostics Taiwan, Inc. - July 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/nipro-diagnostics-taiwan-inc/d0882611-fe79-4167-b29c-a070eb39415d
Source feed: FDA_Inspections

> FDA Inspection 989174 for Nipro Diagnostics Taiwan, Inc. on July 21, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 989174
- Company Name: Nipro Diagnostics Taiwan, Inc.
- Inspection Date: 2016-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 989174 - 2016-07-21](https://www.keypedia.com/records/fda_inspections/nipro-diagnostics-taiwan-inc/b4c98856-df32-4cb4-966e-cbdaf8229159)
- [FDA Inspection 680402 - 2010-08-19](https://www.keypedia.com/records/fda_inspections/nipro-diagnostics-taiwan-inc/65f194ae-6ced-42bd-833f-eb6d41748924)

Company: https://www.keypedia.com/companies/nipro-diagnostics-taiwan-inc/8825d7f4-590b-4b2c-bf03-a60fc6acdebf

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