# FDA Inspection 587890 - Diapulse Corporation of America - June 10, 2009

Source: https://www.keypedia.com/records/fda_inspections/diapulse-corporation-of-america/ae7e1e67-8667-436e-a295-a303c1fc2230
Source feed: FDA_Inspections

> FDA Inspection 587890 for Diapulse Corporation of America on June 10, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 587890
- Company Name: Diapulse Corporation of America
- Inspection Date: 2009-06-10
- 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.keypedia.com/companies/diapulse-corporation-of-america/ba873a45-0aeb-4829-bfd2-836b7d191086

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