# FDA Inspection 1280622 - Keter Canada, Inc. - September 05, 2025

Source: https://www.keypedia.com/records/fda_inspections/keter-canada-inc/a59998da-8fe5-48f0-aa4a-d4aa034b3c26
Source feed: FDA_Inspections

> FDA Inspection 1280622 for Keter Canada, Inc. on September 05, 2025. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280622
- Company Name: Keter Canada, Inc.
- Inspection Date: 2025-09-05
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health

## Related Documents

- [FDA Inspection 1280622 - 2025-09-05](https://www.keypedia.com/records/fda_inspections/keter-canada-inc/a627c4f7-a885-40d0-9a42-fc7c0573807a)
- [FDA Inspection 1280622 - 2025-09-05](https://www.keypedia.com/records/fda_inspections/keter-canada-inc/7f9b3594-c97e-4ad6-854b-c735c2a7173b)
- [FDA Inspection 1280622 - 2025-09-05](https://www.keypedia.com/records/fda_inspections/keter-canada-inc/4c554709-217b-405c-8970-2ab3c4dd2a69)
- [FDA Inspection 1180322 - 2022-09-23](https://www.keypedia.com/records/fda_inspections/keter-canada-inc/6e23e789-8ced-4974-a15a-deca74fd6d09)
- [FDA Inspection 1180322 - 2022-09-23](https://www.keypedia.com/records/fda_inspections/keter-canada-inc/194fc278-c5eb-4b4e-b8fb-5fde655da174)

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