# FDA Inspection 984968 - CLEVERWAVE TECHNOLOGY INC - June 20, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/cleverwave-technology-inc/f85771b6-c491-468f-a08b-e55f1ee992c0/
Source feed: FDA_Inspections

> FDA Inspection 984968 for CLEVERWAVE TECHNOLOGY INC on June 20, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984968
- Company Name: CLEVERWAVE TECHNOLOGY INC
- Inspection Date: 2016-06-20
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 719929 - 2010-11-16](https://www.globalkeysolutions.net/api/records/fda_inspections/cleverwave-technology-inc/6e70e323-e011-4a28-bd59-e57846be4fe2/)
- [FDA Inspection 586852 - 2009-04-10](https://www.globalkeysolutions.net/api/records/fda_inspections/cleverwave-technology-inc/35b9b3dd-b0bd-40ba-b634-164594843e49/)

Company: https://www.globalkeysolutions.net/companies/cleverwave-technology-inc/c6521ec6-93a3-4722-bed0-29a3e9015ff3

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