# FDA Inspection 803599 - Pacific Denshi Co., Ltd. - August 09, 2012

Source: https://www.keypedia.com/records/fda_inspections/pacific-denshi-co-ltd/b2a1146b-8926-4fab-bd3d-7892a3d561d8
Source feed: FDA_Inspections

> FDA Inspection 803599 for Pacific Denshi Co., Ltd. on August 09, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803599
- Company Name: Pacific Denshi Co., Ltd.
- Inspection Date: 2012-08-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 803599 - 2012-08-09](https://www.keypedia.com/records/fda_inspections/pacific-denshi-co-ltd/62a13087-ed01-441e-9221-7ce429bec11f)

Company: https://www.keypedia.com/companies/pacific-denshi-co-ltd/cf966d2e-097a-4ac3-884f-c593015f3304

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