# Laerdal Medical A/S – FDA Inspection, Jun 23, 2011

Source: https://www.keypedia.com/records/fda_inspections/laerdal-medical-as/9c44438c-0673-40ea-9f94-66d00428976b
Source feed: FDA_Inspections

> FDA inspection 738432 of Laerdal Medical A/S, June 23, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 738432
- Company Name: Laerdal Medical A/S
- Inspection Date: 2011-06-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 994026 - 2016-11-10
- [FDA Inspection 845097 - 2013-08-22](https://www.keypedia.com/records/fda_inspections/laerdal-medical-as/62d0a5e3-ce64-4842-8ba6-9895b8356235)

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