# FDA Inspection 1021686 - Bruder Healthcare Company, LLC - August 14, 2017

Source: https://www.keypedia.com/records/fda_inspections/bruder-healthcare-company-llc/204f1623-0cbf-4155-8f98-6a7e1adbe23c
Source feed: FDA_Inspections

> FDA Inspection 1021686 for Bruder Healthcare Company, LLC on August 14, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021686
- Company Name: Bruder Healthcare Company, LLC
- Inspection Date: 2017-08-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/bruder-healthcare-company-llc/b59436a9-a6a3-4129-9809-6d660e6b599b

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