# Sunnex, LLC – FDA Inspection, Jul 3, 2019

Source: https://www.keypedia.com/records/fda_inspections/sunnex-llc/812548dd-e6fa-48c3-b7e5-2f3dbdea4595
Source feed: FDA_Inspections

> FDA inspection 1095148 of Sunnex, LLC, July 03, 2019. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095148
- Company Name: Sunnex, LLC
- Inspection Date: 2019-07-03
- 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: 12

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- FDA Inspection 1162566 - 2022-02-18
- [FDA Inspection 1017642 - 2017-07-12](https://www.keypedia.com/records/fda_inspections/sunnex-llc/86fe1ccc-24db-44fb-bde4-82a285dc77e1)
- [FDA Inspection 916882 - 2015-02-18](https://www.keypedia.com/records/fda_inspections/sunnex-llc/ff27c879-2cc2-488c-8c96-802497d06dc7)
- [FDA Inspection 792958 - 2012-07-30](https://www.keypedia.com/records/fda_inspections/sunnex-llc/8b7b17bc-681e-47e7-97c5-a8945dc4a38c)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

Company: https://www.keypedia.com/companies/sunnex-llc/8a909b31-6bcb-4a15-9c5e-c1f91bb4f858

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