# Eurofins Donor & Product Testing, Inc. Atlanta - Inspection Records

Source: https://www.globalkeysolutions.net/companies/eurofins-donor-product-testing-inc-atlanta/83fcf25f-19a4-4fe5-8cd5-c444c5e6b943

> Inspection records and compliance data for Eurofins Donor & Product Testing, Inc. Atlanta in Marietta, Georgia. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Donor & Product Testing, Inc. Atlanta
- FEI Number: 3012822744
- City: Marietta
- State: Georgia
- Country Name: United States
- Address Line 1: 1700 Enterprise Way Se Ste 114
- Zip Code: 30067

## Related Documents

- [483 - Eurofins Donor & Product Testing, Inc. Atlanta - 2024-11-05](https://www.globalkeysolutions.net/records/483/eurofins-donor-product-testing-inc-atlanta/15d754e4-4fdb-4778-8a3f-53ae27227514) — source: FDA, date: November 5, 2024
- [FDA Inspection 1253795 - Eurofins Donor & Product Testing, Inc. Atlanta - 2024-11-05](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-donor-product-testing-inc-atlanta/444f7d45-62ba-4dee-a922-273e847c64ef) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 5, 2024
- [FDA Inspection 1174965 - Eurofins Donor & Product Testing, Inc. Atlanta - 2022-07-12](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-donor-product-testing-inc-atlanta/877320f9-1447-42a6-a903-1a2e2457ae47) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2022
- [FDA Inspection 1174965 - Eurofins Donor & Product Testing, Inc. Atlanta - 2022-07-12](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-donor-product-testing-inc-atlanta/cdd0b083-5dc8-4fd7-b1f1-06d0d1d8e715) — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2022
- [FDA Inspection 1063364 - Eurofins Donor & Product Testing, Inc. Atlanta - 2018-07-25](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-donor-product-testing-inc-atlanta/ed8d28b1-c6b8-482a-b36b-4a3b1c6983b4) — classification: No Action Indicated (NAI), source: FDA, date: July 25, 2018

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