# FDA Inspection 611182 - Topex Inc - September 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/topex-inc/6789c355-8cfb-4386-9bdb-b5d39b305686
Source feed: FDA_Inspections

> FDA Inspection 611182 for Topex Inc on September 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 611182
- Company Name: Topex Inc
- Inspection Date: 2009-09-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 611182 - 2009-09-09](https://www.keypedia.com/records/fda_inspections/topex-inc/6dad63f7-0e92-4299-a2f5-89e8d2eaa5f4)

Company: https://www.keypedia.com/companies/topex-inc/7bab1752-aad6-4170-9196-cf6a068cdbbc

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