# FDA Inspection 1228351 - THE LINDEN GROUP CORP. - December 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/the-linden-group-corp/6393cee9-75d4-4331-8ff4-8b861cddbd9a
Source feed: FDA_Inspections

> FDA Inspection 1228351 for THE LINDEN GROUP CORP. on December 13, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1228351
- Company Name: THE LINDEN GROUP CORP.
- Inspection Date: 2023-12-13
- 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 1228351 - 2023-12-13](https://www.keypedia.com/records/fda_inspections/the-linden-group-corp/1f8b8113-1fd7-4ebf-9d24-24009ab77de6)

Company: https://www.keypedia.com/companies/the-linden-group-corp/ca78571e-79aa-40e6-a199-14f7d621d915

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