# Bureau Veritas Canada (2019) Inc. - Inspection Records

Source: https://www.keypedia.com/companies/bureau-veritas-canada-2019-inc/c3dc8b08-eccf-4565-8c0b-df0a30f27234

> Inspection records and compliance data for Bureau Veritas Canada (2019) Inc. in Burnaby, None. Access full analysis and detailed observations.

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## Details

- Name: Bureau Veritas Canada (2019) Inc.
- FEI Number: 3008290221
- Canada Business Number: 100938877RC0014
- City: Burnaby
- State: None
- Country Name: Canada
- Address Line 1: 8577 Commerce Crt
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING, CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY, FDF MANUFACTURE, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING

## Related Documents

- [Canada Inspection - Bureau Veritas Canada (2019) Inc. - Inspection #89297 - 2026-06-23](https://www.keypedia.com/records/canada_inspection/bureau-veritas-canada-2019-inc/31f7bcea-2ea5-41cd-baa5-3220109ddd5d) — source: Canada, date: June 23, 2026
- [Canada Inspection - Bureau Veritas Canada (2019) Inc. - Inspection #78086 - 2022-01-19](https://www.keypedia.com/records/canada_inspection/bureau-veritas-canada-2019-inc/9bed7c68-21b0-45b4-9fd2-e650d7f41277) — source: Canada, date: January 19, 2022
- [FDA Inspection 988108 - Bureau Veritas Canada (2019) Inc. - 2016-09-09](https://www.keypedia.com/records/fda_inspections/bureau-veritas-canada-2019-inc/7c4758d5-6811-4ca0-8f8f-6d6586ef306e) — classification: No Action Indicated (NAI), source: FDA, date: September 9, 2016
- [FDA Inspection 873542 - Bureau Veritas Canada (2019) Inc. - 2014-03-12](https://www.keypedia.com/records/fda_inspections/bureau-veritas-canada-2019-inc/b747529e-797e-418e-964a-48dff7fa273d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 12, 2014
- [FDA Inspection 746010 - Bureau Veritas Canada (2019) Inc. - 2011-08-22](https://www.keypedia.com/records/fda_inspections/bureau-veritas-canada-2019-inc/83012143-3085-45bd-97ca-d6af10fd4d51) — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2011

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