# FDA Inspection 1259464 - CDR SYSTEMS, INC. - January 29, 2025

Source: https://www.keypedia.com/records/fda_inspections/cdr-systems-inc/4f5dacfe-a29f-4ac5-b5ed-a309afdf916b
Source feed: FDA_Inspections

> FDA Inspection 1259464 for CDR SYSTEMS, INC. on January 29, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259464
- Company Name: CDR SYSTEMS, INC.
- Inspection Date: 2025-01-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259464 - 2025-01-29](https://www.keypedia.com/records/fda_inspections/cdr-systems-inc/4059a975-f1da-4b34-abee-ef5a9be9858d)
- [FDA Inspection 1049616 - 2018-04-05](https://www.keypedia.com/records/fda_inspections/cdr-systems-inc/1af59950-1666-4bea-94cc-c86bf59a6e22)

Company: https://www.keypedia.com/companies/cdr-systems-inc/e37b68bb-786f-4ebe-85e1-cafa2bae9848

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