# FDA Inspection 1224759 - Memry Corporation - December 01, 2023

Source: https://www.keypedia.com/records/fda_inspections/memry-corporation/7651599f-c485-47a4-bf3a-c3053b0983f1
Source feed: FDA_Inspections

> FDA Inspection 1224759 for Memry Corporation on December 01, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1224759
- Company Name: Memry Corporation
- Inspection Date: 2023-12-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1224759 - 2023-12-01](https://www.keypedia.com/records/fda_inspections/memry-corporation/39eefaac-62c9-4be9-ae74-a22d668148f3)

Company: https://www.keypedia.com/companies/memry-corporation/9de9cfe2-bc1f-4754-b92e-8d27686bfc3e

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