# FDA Inspection 718124 - Aerogen Ltd. - March 31, 2011

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

> FDA Inspection 718124 for Aerogen Ltd. on March 31, 2011. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1062144 - 2018-05-11](https://www.globalkeysolutions.net/records/fda_inspections/aerogen-ltd/c73988a0-3a5a-4e09-8a4b-5d8a53b225b9)
- [FDA Inspection 718124 - 2011-03-31](https://www.globalkeysolutions.net/records/fda_inspections/aerogen-ltd/c04ded76-8189-43a2-b7f1-385671b6ca4a)

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

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