# Aerogen Ltd. – FDA Inspection, Mar 31, 2011

Source: https://www.keypedia.com/records/fda_inspections/aerogen-ltd/df22f61f-b0e1-4910-94ad-aca7480344be
Source feed: FDA_Inspections

> FDA inspection 718124 of Aerogen Ltd., March 31, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 718124
- Company Name: Aerogen Ltd.
- Inspection Date: 2011-03-31
- 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: 1

## Related Documents

- FDA Inspection 1062144 - 2018-05-11

Company: https://www.keypedia.com/companies/aerogen-ltd/275fc6a7-879e-4412-a0fa-19ea63d5ed72

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