# FDA Inspection 994026 - Laerdal Medical A/S - November 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/laerdal-medical-as/a0bd5e94-daa0-4591-95b3-426a472edd27
Source feed: FDA_Inspections

> FDA Inspection 994026 for Laerdal Medical A/S on November 10, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 994026
- Company Name: Laerdal Medical A/S
- Inspection Date: 2016-11-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 845097 - 2013-08-22](https://www.keypedia.com/records/fda_inspections/laerdal-medical-as/62d0a5e3-ce64-4842-8ba6-9895b8356235)
- [FDA Inspection 738432 - 2011-06-23](https://www.keypedia.com/records/fda_inspections/laerdal-medical-as/9c44438c-0673-40ea-9f94-66d00428976b)
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Company: https://www.keypedia.com/companies/laerdal-medical-as/9e58f4ff-ff76-4e29-ae38-f001bf46098e

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