# FDA Inspection 1327210 - Cleveland Diagnostics, Inc - July 20, 2026

Source: https://www.keypedia.com/records/fda_inspections/cleveland-diagnostics-inc/06ee094e-0897-4dec-9a1e-8f688dfc19ca
Source feed: FDA_Inspections

> FDA Inspection 1327210 for Cleveland Diagnostics, Inc on July 20, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1327210
- Company Name: Cleveland Diagnostics, Inc
- Inspection Date: 2026-07-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1327210 - 2026-07-20](https://www.keypedia.com/records/fda_inspections/cleveland-diagnostics-inc/b5c83b51-fee9-48d1-9ab8-8790c839d8dc)
- [FDA Inspection 1163486 - 2022-02-15](https://www.keypedia.com/records/fda_inspections/cleveland-diagnostics-inc/d8fd84e4-e93d-4cbd-ac84-5fa55270e505)

Company: https://www.keypedia.com/companies/cleveland-diagnostics-inc/e532f60c-5bf0-4692-9b5e-760188516e41

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