# FDA Inspection 1242642 - Simpex Medical Inc - June 28, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/simpex-medical-inc/720ee00a-a6cf-49f9-a306-d363ecfcc511
Source feed: FDA_Inspections

> FDA Inspection 1242642 for Simpex Medical Inc on June 28, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1242642
- Company Name: Simpex Medical Inc
- Inspection Date: 2024-06-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1242642 - 2024-06-28](https://www.globalkeysolutions.net/records/fda_inspections/simpex-medical-inc/9652eb5e-bded-46f4-bf14-ded5bfcb1422)
- [FDA Inspection 1102993 - 2019-09-24](https://www.globalkeysolutions.net/records/fda_inspections/simpex-medical-inc/19a33f9f-f045-4cb4-81f2-64e8def84aeb)
- [FDA Inspection 1102993 - 2019-09-24](https://www.globalkeysolutions.net/records/fda_inspections/simpex-medical-inc/cf27a216-a91d-4587-8a4d-e3c7a324aae3)

Company: https://www.globalkeysolutions.net/companies/simpex-medical-inc/a140336e-293a-4625-a8df-c9aecf7ade2b

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