# FDA Inspection 1204021 - MEDISIZE CZ - April 06, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/medisize-cz/748d1632-6848-42a9-aa4a-f06497d19936
Source feed: FDA_Inspections

> FDA Inspection 1204021 for MEDISIZE CZ on April 06, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1204021
- Company Name: MEDISIZE CZ
- Inspection Date: 2023-04-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1204021 - 2023-04-06](https://www.globalkeysolutions.net/records/fda_inspections/medisize-cz/25c0a7d4-af94-448d-abbc-8b4a223e7c5b)
- [FDA Inspection 979367 - 2016-05-27](https://www.globalkeysolutions.net/records/fda_inspections/medisize-cz/fc54dd25-edf3-4069-8e95-34a8ceadc53b)

Company: https://www.globalkeysolutions.net/companies/medisize-cz/b560a3b2-7cd2-4847-8f65-09ec2924c753

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