# FDA Inspection 928436 - Gardner Denver Thomas,  Inc - May 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/gardner-denver-thomas-inc/cda02a06-74d8-424d-981e-0c2ad806a683
Source feed: FDA_Inspections

> FDA Inspection 928436 for Gardner Denver Thomas,  Inc on May 22, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 928436
- Company Name: Gardner Denver Thomas,  Inc
- Inspection Date: 2015-05-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 752076 - 2011-10-31](https://www.keypedia.com/records/fda_inspections/gardner-denver-thomas-inc/5b64c610-9d2f-4acf-9864-a982e584c538)

Company: https://www.keypedia.com/companies/gardner-denver-thomas-inc/b7fbd6e2-95e0-4509-8930-92dc2932ed4b

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