# TD Synnex – FDA Inspection, Apr 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/td-synnex/5d7cbc41-2048-437d-8e1c-7d4fdf5afeda
Source feed: FDA_Inspections

> FDA inspection 1205525 of TD Synnex, April 20, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1205525
- Company Name: TD Synnex
- Inspection Date: 2023-04-20
- 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 Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

Company: https://www.keypedia.com/companies/td-synnex/976737cb-e1ed-4cff-8291-aa0d4c372bf7

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