# Pacific Denshi Co., Ltd. – FDA Inspection, Aug 9, 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 of Pacific Denshi Co., Ltd., August 09, 2012. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803 and 820.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

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
