# FDA Inspection 679641 - Procedure Products, Inc. - August 25, 2010

Source: https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/991e2f2c-26a9-431e-bdeb-52f7086f3b29
Source feed: FDA_Inspections

> FDA Inspection 679641 for Procedure Products, Inc. on August 25, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 679641
- Company Name: Procedure Products, Inc.
- Inspection Date: 2010-08-25
- 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.globalkeysolutions.net/companies/procedure-products-inc/7fd29bd7-1dee-4c43-8b80-d6678a4c6d81

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