# Freudenberg Medical, LLC – FDA Inspection, Jul 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/freudenberg-medical-llc/444d60dd-b6ef-45dc-bf81-1858fd307bfa
Source feed: FDA_Inspections

> FDA inspection 979007 of Freudenberg Medical, LLC, July 22, 2016. Classification: Voluntary Action Indicated (VAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 979007
- Company Name: Freudenberg Medical, LLC
- Inspection Date: 2016-07-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- FDA Inspection 814410 - 2013-01-18
- [FDA Inspection 774360 - 2012-03-27](https://www.keypedia.com/records/fda_inspections/freudenberg-medical-llc/9e39f97b-e5f2-410a-b0f2-95e420596253)
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Company: https://www.keypedia.com/companies/freudenberg-medical-llc/ef21cdf9-4cc6-4f08-aad5-c26dcb1b2a36

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