# FDA Inspection 611026 - Duro-Med Industries - September 03, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/duro-med-industries/17d26bd7-fbab-459e-9ee9-e7baa4d92482
Source feed: FDA_Inspections

> FDA Inspection 611026 for Duro-Med Industries on September 03, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611026
- Company Name: Duro-Med Industries
- Inspection Date: 2009-09-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/duro-med-industries/5513368e-448f-4af8-9700-346b9d21b271

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