# FDA Inspection 1180322 - Keter Canada, Inc. - September 23, 2022

Source: https://www.keypedia.com/records/fda_inspections/keter-canada-inc/194fc278-c5eb-4b4e-b8fb-5fde655da174
Source feed: FDA_Inspections

> FDA Inspection 1180322 for Keter Canada, Inc. on September 23, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180322
- Company Name: Keter Canada, Inc.
- Inspection Date: 2022-09-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/keter-canada-inc/3574e5b0-38b5-4c4d-ac2a-6f638193a3ea

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