# FDA Inspection 742200 - GEXPRO, a Division of REXEL USA Inc - August 26, 2011

Source: https://www.keypedia.com/records/fda_inspections/gexpro-a-division-of-rexel-usa-inc/c9b8f690-57a3-485e-b71f-c31dba22cfc4
Source feed: FDA_Inspections

> FDA Inspection 742200 for GEXPRO, a Division of REXEL USA Inc on August 26, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 742200
- Company Name: GEXPRO, a Division of REXEL USA Inc
- Inspection Date: 2011-08-26
- Classification: No Action Indicated (NAI)
- 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/gexpro-a-division-of-rexel-usa-inc/42a6fefb-6211-4d5d-ba07-1913bd900538

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