# FDA Inspection 1199429 - Cirtec Medical - March 08, 2023

Source: https://www.keypedia.com/records/fda_inspections/cirtec-medical/f2848b9e-8e18-4021-b48d-49563a734c0d
Source feed: FDA_Inspections

> FDA Inspection 1199429 for Cirtec Medical on March 08, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199429
- Company Name: Cirtec Medical
- Inspection Date: 2023-03-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199429 - 2023-03-08](https://www.keypedia.com/records/fda_inspections/cirtec-medical/7512692b-9431-463c-b639-28a0d215863b)
- [FDA Inspection 1122361 - 2020-01-27](https://www.keypedia.com/records/fda_inspections/cirtec-medical/4b84d4bc-25e3-49b0-a3bd-0c8503f5f2f8)
- [FDA Inspection 1122361 - 2020-01-27](https://www.keypedia.com/records/fda_inspections/cirtec-medical/c7bfd740-26d4-4f3a-8c10-2c0b3528bb16)

Company: https://www.keypedia.com/companies/cirtec-medical/f70ce84f-f01e-4b23-8cd5-2046b4ecb70e

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