# FDA Inspection 959099 - Gunnell Llc - February 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/gunnell-llc/6853ca6d-c13d-4019-90df-9949f6885e35
Source feed: FDA_Inspections

> FDA Inspection 959099 for Gunnell Llc on February 18, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 959099
- Company Name: Gunnell Llc
- Inspection Date: 2016-02-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 959099 - 2016-02-18](https://www.keypedia.com/records/fda_inspections/gunnell-llc/959679f2-09f5-446e-9641-0b88b9c5c7e0)
- [FDA Inspection 793234 - 2012-08-24](https://www.keypedia.com/records/fda_inspections/gunnell-llc/59c9a640-0058-4f46-a730-adff193d37f5)
- [FDA Inspection 732620 - 2011-06-23](https://www.keypedia.com/records/fda_inspections/gunnell-llc/723cab16-52da-4e6b-bef1-a1baaae16791)
- [FDA Inspection 670779 - 2010-06-30](https://www.keypedia.com/records/fda_inspections/gunnell-llc/6ad0a878-76ed-4502-8145-64aa9441b22a)

Company: https://www.keypedia.com/companies/gunnell-llc/f118929d-72c5-4b43-bca7-ee1a4f559704

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