# Carter BloodCare - Tyler, Tyler, TX – FDA Inspections

Source: https://www.keypedia.com/companies/carter-bloodcare-tyler/dc81e28f-3ee5-4b46-92ec-04901dd3199b

> Inspection records and compliance data for Carter BloodCare - Tyler in Tyler, Texas. 7 FDA inspections on record, last inspected March 07, 2025.

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## Details

- Name: Carter BloodCare - Tyler
- FEI Number: 1672331
- Address Line 1: 815 S Baxter Ave
- City: Tyler
- State: Texas
- Zip Code: 75701
- Country Name: United States
- Address: 815 S Baxter Ave, Tyler, Texas 75701, United States
- Country: United States

## Related Documents

- FDA Inspection 1264020 - Carter BloodCare - Tyler - 2025-03-07 — source: FDA, date: March 7, 2025
- FDA Inspection 1264020 - Carter BloodCare - Tyler - 2025-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2025
- FDA Inspection 1173367 - Carter BloodCare - Tyler - 2022-06-16 — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2022
- FDA Inspection 1173367 - Carter BloodCare - Tyler - 2022-06-16 — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2022
- FDA Inspection 1041185 - Carter BloodCare - Tyler - 2018-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2018
- [FDA Inspection 974966 - Carter BloodCare - Tyler - 2016-06-01](https://www.keypedia.com/records/fda_inspections/carter-bloodcare-tyler/ce943196-1cb0-49c1-a00d-65431596f973) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2016
- FDA Inspection 883573 - Carter BloodCare - Tyler - 2014-06-06 — classification: No Action Indicated (NAI), source: FDA, date: June 6, 2014
- FDA Inspection 764424 - Carter BloodCare - Tyler - 2012-01-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 20, 2012
- [FDA Inspection 625989 - Carter BloodCare - Tyler - 2009-10-20](https://www.keypedia.com/records/fda_inspections/carter-bloodcare-tyler/01628e80-f19b-4f9a-b24a-855bb203481c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 20, 2009

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