# FDA Inspection 913129 - Gardner Denver Thomas Inc - February 06, 2015

Source: https://www.keypedia.com/records/fda_inspections/gardner-denver-thomas-inc/397e362f-0f05-46a4-bd62-5a8c8e55d17f
Source feed: FDA_Inspections

> FDA Inspection 913129 for Gardner Denver Thomas Inc on February 06, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 913129
- Company Name: Gardner Denver Thomas Inc
- Inspection Date: 2015-02-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 737266 - 2011-08-03](https://www.keypedia.com/records/fda_inspections/gardner-denver-thomas-inc/5960cc50-9d83-49f5-b35e-a93447ed015e)

Company: https://www.keypedia.com/companies/gardner-denver-thomas-inc/56134459-b6ce-41f2-9f26-6f1ba598df41

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