# FDA Inspection 1202315 - InterCare DX, Inc - March 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/intercare-dx-inc/75d8d2ec-8e01-4860-9ebf-97dc5a896f06
Source feed: FDA_Inspections

> FDA Inspection 1202315 for InterCare DX, Inc on March 27, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1202315
- Company Name: InterCare DX, Inc
- Inspection Date: 2023-03-27
- 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 1202315 - 2023-03-27](https://www.keypedia.com/records/fda_inspections/intercare-dx-inc/ecfdef87-bbb4-46a2-8cf4-870c6eea4730)
- [FDA Inspection 747292 - 2011-09-27](https://www.keypedia.com/records/fda_inspections/intercare-dx-inc/d6109113-1114-435f-b87b-bda2f0436c1a)

Company: https://www.keypedia.com/companies/intercare-dx-inc/caf4439f-3027-4791-bd63-515f72868b0e

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