# InterCare DX, Inc – FDA Inspection, Mar 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/intercare-dx-inc/ecfdef87-bbb4-46a2-8cf4-870c6eea4730
Source feed: FDA_Inspections

> FDA inspection 1202315 of InterCare DX, Inc, March 27, 2023. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Citation Count: 0

## Related Documents

- FDA Inspection 747292 - 2011-09-27

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

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