# FDA Inspection 1238116 - Garaventa (Canada), Ltd. - May 09, 2024

Source: https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/6d2fc4bb-cb2d-409c-911a-d3fe138a7381
Source feed: FDA_Inspections

> FDA Inspection 1238116 for Garaventa (Canada), Ltd. on May 09, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1238116
- Company Name: Garaventa (Canada), Ltd.
- Inspection Date: 2024-05-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1238116 - 2024-05-09](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/48bed580-723e-49c3-b917-461d3c8ff557)
- [FDA Inspection 1038581 - 2018-01-18](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/a32841cf-ef0d-4106-ac80-49d40802b302)
- [FDA Inspection 1038581 - 2018-01-18](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/af50309f-d921-40de-ab01-9223c7108690)
- [FDA Inspection 809444 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/8787c210-212c-440d-abd9-2819ab96e2b0)

Company: https://www.keypedia.com/companies/garaventa-canada-ltd/a7e54e05-2d0b-49cf-b757-912db984d15a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7