# Tokyo Boeki Medisys, Inc. – FDA Inspection, Mar 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/tokyo-boeki-medisys-inc/ccbdde21-c773-4e94-9ace-61a23b0d9b7b
Source feed: FDA_Inspections

> FDA inspection 1009378 of Tokyo Boeki Medisys, Inc., March 24, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009378
- Company Name: Tokyo Boeki Medisys, Inc.
- Inspection Date: 2017-03-24
- 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: 6

## Related Documents

- [FDA Inspection 868114 - 2014-02-27](https://www.keypedia.com/records/fda_inspections/tokyo-boeki-medisys-inc/2c761244-b13f-4c9a-947f-3e927de38d29)

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/tokyo-boeki-medisys-inc/6b1c2d80-9c70-4415-95a8-db3912d9eb10

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