# FDA Inspection 787159 - Laerdal Medical Corporation - June 13, 2012

Source: https://www.keypedia.com/records/fda_inspections/laerdal-medical-corporation/120eec56-59b7-44ef-88f7-19b906c8a87f
Source feed: FDA_Inspections

> FDA Inspection 787159 for Laerdal Medical Corporation on June 13, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 787159
- Company Name: Laerdal Medical Corporation
- Inspection Date: 2012-06-13
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 787159 - 2012-06-13](https://www.keypedia.com/records/fda_inspections/laerdal-medical-corporation/b2e5de57-7f51-4076-977d-bf470cf5a0d1)

Company: https://www.keypedia.com/companies/laerdal-medical-corporation/033f97bb-ce0d-42f8-9a52-8b58579f5f42

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