# Alcon Grieshaber AG – FDA Inspection, Apr 14, 2011

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

> FDA inspection 722909 of Alcon Grieshaber AG, April 14, 2011. Classification: Voluntary Action Indicated (VAI). 4 citations 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: 722909
- Company Name: Alcon Grieshaber AG
- Inspection Date: 2011-04-14
- 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: 4

## Related Documents

- FDA Inspection 914434 - 2015-02-19

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

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