# FDA Inspection 732620 - Gunnell Llc - June 23, 2011

Source: https://www.keypedia.com/records/fda_inspections/gunnell-llc/723cab16-52da-4e6b-bef1-a1baaae16791
Source feed: FDA_Inspections

> FDA Inspection 732620 for Gunnell Llc on June 23, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 732620
- Company Name: Gunnell Llc
- Inspection Date: 2011-06-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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