# Turbochef Technologies Inc – FDA Inspection, Mar 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/turbochef-technologies-inc/02930630-e185-4bc9-9c40-e51ae1181e37
Source feed: FDA_Inspections

> FDA inspection 1009119 of Turbochef Technologies Inc, March 28, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 1010 and 1030. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009119
- Company Name: Turbochef Technologies Inc
- Inspection Date: 2017-03-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- Issuing Officer
- Issuing Officer
- Issuing Officer

Company: https://www.keypedia.com/companies/turbochef-technologies-inc/1595558d-3244-4e0f-9190-3ec4128118fd

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