# FDA Inspection 616834 - Eriez Manufacturing Co - September 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/eriez-manufacturing-co/cdbc0bdf-122b-4f59-872d-b04340f9c02b
Source feed: FDA_Inspections

> FDA Inspection 616834 for Eriez Manufacturing Co on September 28, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 616834
- Company Name: Eriez Manufacturing Co
- Inspection Date: 2009-09-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/eriez-manufacturing-co/beea48c1-4335-4d20-b278-b46a55fb990a

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