# Vitalant Reference and Transfusion Service - Inspection Records

Source: https://www.globalkeysolutions.net/companies/vitalant-reference-and-transfusion-service/e2eb1e52-ffce-4ac7-8c0b-47d1fc40b499

> Inspection records and compliance data for Vitalant Reference and Transfusion Service in Monroeville, Pennsylvania. Access full analysis and detailed observations.

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## Details

- Name: Vitalant Reference and Transfusion Service
- FEI Number: 3005010745
- City: Monroeville
- State: Pennsylvania
- Country Name: United States
- Address Line 1: Forbes Regional Hospital, 2570 Haymaker Rd
- Zip Code: 15146

## Related Documents

- [FDA Inspection 1037237 - Vitalant Reference and Transfusion Service - 2018-01-10](https://www.globalkeysolutions.net/records/fda_inspections/vitalant-reference-and-transfusion-service/fe45ec2c-ccb3-4e6a-9804-0a9d56ef450a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 10, 2018
- [FDA Inspection 865604 - Vitalant Reference and Transfusion Service - 2014-02-11](https://www.globalkeysolutions.net/records/fda_inspections/vitalant-reference-and-transfusion-service/1f9d6ad3-14f0-4213-9860-65db456c9be3) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2014
- [FDA Inspection 767067 - Vitalant Reference and Transfusion Service - 2012-02-09](https://www.globalkeysolutions.net/records/fda_inspections/vitalant-reference-and-transfusion-service/79169871-d335-4001-91d5-99bc75134cac) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2012
- [FDA Inspection 649374 - Vitalant Reference and Transfusion Service - 2010-03-03](https://www.globalkeysolutions.net/records/fda_inspections/vitalant-reference-and-transfusion-service/fc87c703-6c31-4c76-a7c5-2528c28c081a) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2010
- [FDA Inspection 545391 - Vitalant Reference and Transfusion Service - 2008-11-04](https://www.globalkeysolutions.net/records/fda_inspections/vitalant-reference-and-transfusion-service/8aa3e649-47b0-4508-a1b5-97b98408e31c) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2008

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