# Innovative Blood Resources, Lincoln, NE – FDA Inspections

Source: https://www.keypedia.com/companies/innovative-blood-resources/44bc20e8-cfc2-4fd5-afce-d139817e64bd

> Inspection records and compliance data for Innovative Blood Resources in Lincoln, Nebraska. 9 FDA inspections on record, last inspected June 03, 2026.

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## Details

- Name: Innovative Blood Resources
- FEI Number: 3003294594
- Address Line 1: 1631 Pine Lake Rd
- City: Lincoln
- State: Nebraska
- Zip Code: 68512
- Country Name: United States
- Address: 1631 Pine Lake Rd, Lincoln, Nebraska 68512, United States
- Country: United States

## Related Documents

- FDA Inspection 1321522 - Innovative Blood Resources - 2026-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2026
- FDA Inspection 1194208 - Innovative Blood Resources - 2022-12-14 — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2022
- FDA Inspection 1194208 - Innovative Blood Resources - 2022-12-14 — classification: No Action Indicated (NAI), source: FDA, date: December 14, 2022
- FDA Inspection 1099476 - Innovative Blood Resources - 2019-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2019
- FDA Inspection 990229 - Innovative Blood Resources - 2016-10-06 — classification: No Action Indicated (NAI), source: FDA, date: October 6, 2016
- FDA Inspection 902219 - Innovative Blood Resources - 2014-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2014
- FDA Inspection 852967 - Innovative Blood Resources - 2013-10-16 — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2013
- FDA Inspection 797516 - Innovative Blood Resources - 2012-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2012
- FDA Inspection 676199 - Innovative Blood Resources - 2010-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2010
- FDA Inspection 592885 - Innovative Blood Resources - 2009-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2009

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