# Sanuwave Inc – FDA Inspection, Dec 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/sanuwave-inc/75133e96-6c51-4f81-819d-4fdbcc5ee794
Source feed: FDA_Inspections

> FDA inspection 907399 of Sanuwave Inc, December 15, 2014. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 907399
- Company Name: Sanuwave Inc
- Inspection Date: 2014-12-15
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1041626 - 2018-01-10
- FDA Inspection 962343 - 2016-02-17
- FDA Inspection 756365 - 2011-12-06
- FDA Inspection 750410 - 2011-10-19
- FDA Inspection 611061 - 2009-09-10

Company: https://www.keypedia.com/companies/sanuwave-inc/056374b0-b3b4-4399-969a-9c2a0b69e1c2

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