# FDA Inspection 878599 - Dune Medical Devices, Ltd - March 27, 2014

Source: https://www.keypedia.com/records/fda_inspections/dune-medical-devices-ltd/097d8dc2-0a82-467c-a71f-aaadf2d08ea1
Source feed: FDA_Inspections

> FDA Inspection 878599 for Dune Medical Devices, Ltd on March 27, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 878599
- Company Name: Dune Medical Devices, Ltd
- Inspection Date: 2014-03-27
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 878599 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/dune-medical-devices-ltd/c331949e-87c6-4e73-850f-a2cabe1dfb86)
- [FDA Inspection 783565 - 2012-04-24](https://www.keypedia.com/records/fda_inspections/dune-medical-devices-ltd/d51b73bb-87a8-4ca6-a522-5bb5dc97b91f)

Company: https://www.keypedia.com/companies/dune-medical-devices-ltd/91f7f792-66a7-467f-aaf1-b24d78851c93

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