# FDA Inspection 962521 - M.e. Nikkiso Company Ltd. - February 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/me-nikkiso-company-ltd/972e74cb-a2ae-47aa-a4c5-e507e72ccdd1
Source feed: FDA_Inspections

> FDA Inspection 962521 for M.e. Nikkiso Company Ltd. on February 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 962521
- Company Name: M.e. Nikkiso Company Ltd.
- Inspection Date: 2016-02-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 962521 - 2016-02-18](https://www.keypedia.com/records/fda_inspections/me-nikkiso-company-ltd/5afe24a3-0074-4c84-94d3-bfd72d7ee3c5)
- [FDA Inspection 728053 - 2011-05-26](https://www.keypedia.com/records/fda_inspections/me-nikkiso-company-ltd/c8df6234-55ea-4c42-9dc6-959c43a4f477)
- [FDA Inspection 728053 - 2011-05-26](https://www.keypedia.com/records/fda_inspections/me-nikkiso-company-ltd/91e34014-2e71-43cc-9e43-11d81b934db6)

Company: https://www.keypedia.com/companies/me-nikkiso-company-ltd/2309fff3-6fca-46c5-849d-409d9d29b106

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