# FDA Inspection 868473 - Denka Seiken Co., Ltd. - Niigata Factory - February 13, 2014

Source: https://www.keypedia.com/records/fda_inspections/denka-seiken-co-ltd-niigata-factory/7db0e93f-af9e-4f77-a9e2-1e2693f6f535
Source feed: FDA_Inspections

> FDA Inspection 868473 for Denka Seiken Co., Ltd. - Niigata Factory on February 13, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 868473
- Company Name: Denka Seiken Co., Ltd. - Niigata Factory
- Inspection Date: 2014-02-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/denka-seiken-co-ltd-niigata-factory/58990739-9318-428f-9454-5b515d49cb53

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