# Laerdal Medical (Suzhou) Co., Ltd. – FDA Inspection, Jun 6, 2013

Source: https://www.keypedia.com/records/fda_inspections/laerdal-medical-suzhou-co-ltd/d3f60d62-da7b-4b33-9bea-c50f5a50d592
Source feed: FDA_Inspections

> FDA inspection 838796 of Laerdal Medical (Suzhou) Co., Ltd., June 06, 2013. 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: 838796
- Company Name: Laerdal Medical (Suzhou) Co., Ltd.
- Inspection Date: 2013-06-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1029850 - 2016-11-03
- [FDA Inspection 660424 - 2010-04-28](https://www.keypedia.com/records/fda_inspections/laerdal-medical-suzhou-co-ltd/ccfee141-2f3c-48ca-bd6a-dffee28fadc5)

Company: https://www.keypedia.com/companies/laerdal-medical-suzhou-co-ltd/6b6d0262-27cf-4d51-9874-f5e77f66230e

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