# Gunnell Llc – FDA Inspection, Jun 30, 2010

Source: https://www.keypedia.com/records/fda_inspections/gunnell-llc/6ad0a878-76ed-4502-8145-64aa9441b22a
Source feed: FDA_Inspections

> FDA inspection 670779 of Gunnell Llc, June 30, 2010. Classification: Official Action Indicated (OAI). 11 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 670779
- Company Name: Gunnell Llc
- Inspection Date: 2010-06-30
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- FDA Inspection 959099 - 2016-02-18
- [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)

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