# Quality Assistance SA - Inspection Records

Source: https://www.keypedia.com/companies/quality-assistance-sa/707c8a0a-0d4e-4299-beff-f884ad89b4ef

> Inspection records and compliance data for Quality Assistance SA in Thuin, None. Access full analysis and detailed observations.

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## Details

- Name: Quality Assistance SA
- FEI Number: 3002367943
- City: Thuin
- State: None
- Country Name: Belgium
- Address Line 1: Technoparc de Thudinie 2
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1302340 - Quality Assistance SA - 2025-09-04](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/90d90a16-fef3-4bd2-89db-eb1cccfa7b2a) — source: FDA, date: September 4, 2025
- [FDA Inspection 1302340 - Quality Assistance SA - 2025-09-04](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/e915b05d-8e79-485f-a346-106865d6e826) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 4, 2025
- [FDA Inspection 1278764 - Quality Assistance SA - 2021-02-12](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/b96c6d1d-1877-4884-8b66-3a3336ab136e) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2021
- [FDA Inspection 1102275 - Quality Assistance SA - 2019-09-17](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/3e38d625-2b52-406f-8fbb-720b90dd48da) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2019
- [FDA Inspection 885462 - Quality Assistance SA - 2014-06-04](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/4919d5cc-73ec-46b3-8aac-fe7bb9fe1c75) — classification: No Action Indicated (NAI), source: FDA, date: June 4, 2014
- [FDA Inspection 651125 - Quality Assistance SA - 2010-02-16](https://www.keypedia.com/records/fda_inspections/quality-assistance-sa/20675874-fcef-4147-a389-fe45c519e07a) — classification: No Action Indicated (NAI), source: FDA, date: February 16, 2010

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