# Thrombolex Inc – FDA Inspection, Mar 30, 2023

Source: https://www.keypedia.com/records/fda_inspections/thrombolex-inc/5201dfab-0ae0-41a0-bdcf-7f3d290eec5f
Source feed: FDA_Inspections

> FDA inspection 1201201 of Thrombolex Inc, March 30, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 803. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1201201
- Company Name: Thrombolex Inc
- Inspection Date: 2023-03-30
- 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: 2

## Related Documents

- FDA Inspection 1308330 - 2026-03-13

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)

Company: https://www.keypedia.com/companies/thrombolex-inc/51351603-818c-4f4e-88d7-635937ee1a9d

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