# FDA Inspection 1024232 - Eurofins Donor & Product Testing Inc Dallas - August 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc-dallas/4bc6f23b-d3eb-4cc1-b941-8c5caf3f86d7
Source feed: FDA_Inspections

> FDA Inspection 1024232 for Eurofins Donor & Product Testing Inc Dallas on August 09, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024232
- Company Name: Eurofins Donor & Product Testing Inc Dallas
- Inspection Date: 2017-08-09
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

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Company: https://www.keypedia.com/companies/eurofins-donor-product-testing-inc-dallas/aadf26a0-1df2-4db9-8842-73a366ae0bdb

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d