# Sanyo Tokyo Manufacturing Co., Ltd. – FDA Inspection, Jan 27, 2011

Source: https://www.keypedia.com/records/fda_inspections/sanyo-tokyo-manufacturing-co-ltd/976e633e-56e5-47ef-8ede-5cb63dece0b1
Source feed: FDA_Inspections

> FDA inspection 710527 of Sanyo Tokyo Manufacturing Co., Ltd., January 27, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 710527
- Company Name: Sanyo Tokyo Manufacturing Co., Ltd.
- Inspection Date: 2011-01-27
- 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: 2

Company: https://www.keypedia.com/companies/sanyo-tokyo-manufacturing-co-ltd/3448debf-0753-4b3c-b1d6-8743969db123

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