# FDA Inspection 809211 - Dynawave Corp - December 05, 2012

Source: https://www.keypedia.com/records/fda_inspections/dynawave-corp/473d852c-28ef-4e76-99af-c6ef0c0373b6
Source feed: FDA_Inspections

> FDA Inspection 809211 for Dynawave Corp on December 05, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809211
- Company Name: Dynawave Corp
- Inspection Date: 2012-12-05
- 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/dynawave-corp/495dc75d-66d2-4373-af2e-84dba2640ff6

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