# FDA Inspection 892021 - Dorel Juvenile Group, Inc. - August 20, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/dorel-juvenile-group-inc/fc72579a-c684-4e41-babc-8e4337ce74aa/
Source feed: FDA_Inspections

> FDA Inspection 892021 for Dorel Juvenile Group, Inc. on August 20, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 892021
- Company Name: Dorel Juvenile Group, Inc.
- Inspection Date: 2014-08-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 892021 - 2014-08-20](https://www.globalkeysolutions.net/api/records/fda_inspections/dorel-juvenile-group-inc/1e2c2b12-5b7a-47ed-9f11-2330bfb3585e/)
- [FDA Inspection 733498 - 2011-07-01](https://www.globalkeysolutions.net/api/records/fda_inspections/dorel-juvenile-group-inc/795e67f1-8a0f-4939-a1a6-17e36ac5f81c/)

Company: https://www.globalkeysolutions.net/companies/dorel-juvenile-group-inc/4fbcc858-59fe-4329-9a01-029bbd865971

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