# FDA Inspection 908610 - Procedure Products, Inc. - January 05, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/procedure-products-inc/0d19a56d-a1d9-4694-b0a5-24ad581ea07a
Source feed: FDA_Inspections

> FDA Inspection 908610 for Procedure Products, Inc. on January 05, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 908610
- Company Name: Procedure Products, Inc.
- Inspection Date: 2015-01-05
- Classification: No Action Indicated (NAI)
- 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/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