# FDA Inspection 930410 - Rondex Products, Inc. - June 02, 2015

Source: https://www.keypedia.com/records/fda_inspections/rondex-products-inc/19351287-a600-4e7e-a9af-879d30186ef5
Source feed: FDA_Inspections

> FDA Inspection 930410 for Rondex Products, Inc. on June 02, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930410
- Company Name: Rondex Products, Inc.
- Inspection Date: 2015-06-02
- 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/rondex-products-inc/dc7ea51f-4e39-44cf-8d85-7eaaaf85cd84

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