# FDA Inspection 1088025 - Kluge Design Inc. - April 15, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kluge-design-inc/a0bb7f79-12a3-4d41-9681-1cf34b59f948
Source feed: FDA_Inspections

> FDA Inspection 1088025 for Kluge Design Inc. on April 15, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088025
- Company Name: Kluge Design Inc.
- Inspection Date: 2019-04-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 952982 - 2015-12-11](https://www.globalkeysolutions.net/records/fda_inspections/kluge-design-inc/64d4aae2-7d8c-489e-9c49-b2c5139baa4c)

Company: https://www.globalkeysolutions.net/companies/kluge-design-inc/f08e1bc1-ddb9-4ae7-9422-80184a18b4c1

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