# Torbot Group, Inc. – FDA Inspection, Sep 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/torbot-group-inc/0c6308ba-9a20-49d2-90a3-fca12cf10b91
Source feed: FDA_Inspections

> FDA inspection 614577 of Torbot Group, Inc., September 23, 2009. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 614577
- Company Name: Torbot Group, Inc.
- Inspection Date: 2009-09-23
- 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 893627 - 2014-08-28](https://www.keypedia.com/records/fda_inspections/torbot-group-inc/47a02c8f-46e2-4b75-977d-9e70d482e24c)
- [FDA Inspection 772108 - 2012-03-02](https://www.keypedia.com/records/fda_inspections/torbot-group-inc/8fa3ee55-f495-4c0e-aa4e-9d42014fcd93)

Company: https://www.keypedia.com/companies/torbot-group-inc/18e8c1f3-d12d-4c29-848f-79158f88ca5e

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