# FDA Inspection 956228 - Tochigi Seiko Kk - December 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/tochigi-seiko-kk/87878381-7d93-4007-a46f-013e6a73c4c1
Source feed: FDA_Inspections

> FDA Inspection 956228 for Tochigi Seiko Kk on December 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 956228
- Company Name: Tochigi Seiko Kk
- Inspection Date: 2015-12-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/tochigi-seiko-kk/84ae4b7b-60b9-4059-88af-590e87af3959

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