# Syneos Health Clinique, Inc., Quebec, Canada – FDA Inspections

Source: https://www.keypedia.com/companies/syneos-health-clinique-inc/0711d0d4-5c77-44f7-a7f2-74bae0672f7f

> Inspection records and compliance data for Syneos Health Clinique, Inc. in Quebec. 8 FDA inspections on record, last inspected September 12, 2025.

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## Details

- Name: Syneos Health Clinique, Inc.
- FEI Number: 3002533384
- Business Operations: CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING
- Address Line 1: 2500 Einstein St
- City: Quebec
- Country Name: Canada
- Address: 2500 Einstein St, Quebec, Canada
- Country: Canada

## Related Documents

- FDA Inspection 1294546 - Syneos Health Clinique, Inc. - 2025-09-12 — source: FDA, date: September 12, 2025
- FDA Inspection 1294546 - Syneos Health Clinique, Inc. - 2025-09-12 — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2025
- FDA Inspection 1195997 - Syneos Health Clinique, Inc. - 2023-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2023
- [FDA Inspection 1114335 - Syneos Health Clinique, Inc. - 2019-12-13](https://www.keypedia.com/records/fda_inspections/syneos-health-clinique-inc/3b965e9a-6139-4e73-a9e7-e7292e9fecd8) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2019
- FDA Inspection 1100542 - Syneos Health Clinique, Inc. - 2019-06-28 — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2019
- [FDA Inspection 1097875 - Syneos Health Clinique, Inc. - 2019-06-14](https://www.keypedia.com/records/fda_inspections/syneos-health-clinique-inc/17f06321-8c4f-4b10-b623-e7232f98b65d) — classification: No Action Indicated (NAI), source: FDA, date: June 14, 2019
- FDA Inspection 1010210 - Syneos Health Clinique, Inc. - 2017-04-07 — source: FDA, date: April 7, 2017
- FDA Inspection 1004074 - Syneos Health Clinique, Inc. - 2017-02-10 — source: FDA, date: February 10, 2017
- FDA Inspection 1005082 - Syneos Health Clinique, Inc. - 2017-02-03 — source: FDA, date: February 3, 2017

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