# Garaventa (Canada), Ltd. – FDA Inspection, Jan 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/af50309f-d921-40de-ab01-9223c7108690
Source feed: FDA_Inspections

> FDA inspection 1038581 of Garaventa (Canada), Ltd., January 18, 2018. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038581
- Company Name: Garaventa (Canada), Ltd.
- Inspection Date: 2018-01-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 9

## Related Documents

- [FDA Inspection 1238116 - 2024-05-09](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/6d2fc4bb-cb2d-409c-911a-d3fe138a7381)
- [FDA Inspection 809444 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/garaventa-canada-ltd/8787c210-212c-440d-abd9-2819ab96e2b0)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/tania-e-vizcaino/a142e189-697e-4962-97a9-8d24a52d690e)

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