# FDA Inspection 1201201 - Thrombolex Inc - March 30, 2023

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

> FDA Inspection 1201201 for Thrombolex Inc on March 30, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1308330 - 2026-03-13](https://www.keypedia.com/records/fda_inspections/thrombolex-inc/e69b757c-1c1e-4803-b6d7-1c492f005cbe)
- [FDA Inspection 1308330 - 2026-03-13](https://www.keypedia.com/records/fda_inspections/thrombolex-inc/70b5d6ec-540e-4f6a-a12b-cadea8e99e30)

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