# FDA Inspection 883853 - Kulzer, LLC. - June 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/kulzer-llc/4f41b8d7-aca6-4edc-8a3e-42452f574b4e
Source feed: FDA_Inspections

> FDA Inspection 883853 for Kulzer, LLC. on June 20, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 883853
- Company Name: Kulzer, LLC.
- Inspection Date: 2014-06-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/kulzer-llc/35c53baa-9b43-462a-ab99-f4636a5dec03

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