# DonorConnect - Inspection Records

Source: https://www.globalkeysolutions.net/companies/donorconnect/d7959cda-d542-4f62-bfc3-e93f72864651

> Inspection records and compliance data for DonorConnect in Salt Lake City, Utah. Access full analysis and detailed observations.

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## Details

- Name: DonorConnect
- FEI Number: 3000215350
- City: Salt Lake City
- State: Utah
- Country Name: United States
- Address Line 1: 230 S 500 E Ste 490
- Zip Code: 84102

## Related Documents

- [FDA Inspection 1282450 - DonorConnect - 2025-09-05](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/8cb1fc4c-4450-421a-83c2-3a963fc1be77) — source: FDA, date: September 5, 2025
- [FDA Inspection 1282450 - DonorConnect - 2025-09-05](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/6970b40a-392a-4a75-98dd-0d1219c95d99) — classification: No Action Indicated (NAI), source: FDA, date: September 5, 2025
- [FDA Inspection 1100689 - DonorConnect - 2019-08-20](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/bed1146b-01cd-4f66-b1c0-7a6b5dd7c8f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 20, 2019
- [FDA Inspection 980883 - DonorConnect - 2016-06-22](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/2221f62e-3d8e-433e-8193-68917638181b) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2016
- [FDA Inspection 823576 - DonorConnect - 2013-03-14](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/fbd64e7f-c7a3-4f95-baff-1381fabd5c26) — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2013
- [FDA Inspection 773542 - DonorConnect - 2012-03-08](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/6a36feea-98e0-4422-b75a-b3a539f210bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2012
- [FDA Inspection 622838 - DonorConnect - 2009-10-26](https://www.globalkeysolutions.net/records/fda_inspections/donorconnect/0ed3c506-6a61-4046-b7b0-e7c3a38d8197) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2009

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