# FDA Inspection 722909 - Alcon Grieshaber AG - April 14, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/alcon-grieshaber-ag/ff2542bf-2b9f-40a9-99d5-6090efa522b7/
Source feed: FDA_Inspections

> FDA Inspection 722909 for Alcon Grieshaber AG on April 14, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 722909
- Company Name: Alcon Grieshaber AG
- Inspection Date: 2011-04-14
- 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 914434 - 2015-02-19](https://www.globalkeysolutions.net/api/records/fda_inspections/alcon-grieshaber-ag/f110597d-a14b-48b1-ba08-425266fb4f45/)
- [FDA Inspection 722909 - 2011-04-14](https://www.globalkeysolutions.net/api/records/fda_inspections/alcon-grieshaber-ag/c30c5762-5ce8-4394-a97f-1c08ade8e9e3/)

Company: https://www.globalkeysolutions.net/companies/alcon-grieshaber-ag/5dd813bf-aa78-4c31-9211-d6dcf99c5bbd

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