# General Devices Llc – FDA Inspection, Jul 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/general-devices-llc/dcf2dd96-0a03-42b5-ae17-1513dbcfd255
Source feed: FDA_Inspections

> FDA inspection 678182 of General Devices Llc, July 29, 2010. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 678182
- Company Name: General Devices Llc
- Inspection Date: 2010-07-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1018328 - 2017-03-30
- [FDA Inspection 931039 - 2015-06-11](https://www.keypedia.com/records/fda_inspections/general-devices-llc/7240be77-4617-4f28-b5b6-ec17e8b25f48)
- FDA Inspection 812713 - 2012-12-14

Company: https://www.keypedia.com/companies/general-devices-llc/2ab2cc56-b870-4fc9-9a3f-f8bd76bc5cea

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