# FDA Inspection 914434 - Alcon Grieshaber AG - February 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/alcon-grieshaber-ag/f110597d-a14b-48b1-ba08-425266fb4f45
Source feed: FDA_Inspections

> FDA Inspection 914434 for Alcon Grieshaber AG on February 19, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 914434
- Company Name: Alcon Grieshaber AG
- Inspection Date: 2015-02-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 722909 - 2011-04-14](https://www.keypedia.com/records/fda_inspections/alcon-grieshaber-ag/ff2542bf-2b9f-40a9-99d5-6090efa522b7)
- [FDA Inspection 722909 - 2011-04-14](https://www.keypedia.com/records/fda_inspections/alcon-grieshaber-ag/c30c5762-5ce8-4394-a97f-1c08ade8e9e3)

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