# Alcon LenSx, Inc. – FDA Inspection, Feb 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/alcon-lensx-inc/d093f6a3-b45e-4aee-b34d-3334a0d665d7
Source feed: FDA_Inspections

> FDA inspection 865838 of Alcon LenSx, Inc., February 10, 2014. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803, 806 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 865838
- Company Name: Alcon LenSx, Inc.
- Inspection Date: 2014-02-10
- 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: 5

## Related Documents

- [FDA Inspection 793453 - 2012-08-02](https://www.keypedia.com/records/fda_inspections/alcon-lensx-inc/74f839fd-880a-4d40-ab66-c5c8e0e924be)

Company: https://www.keypedia.com/companies/alcon-lensx-inc/41ae4929-7f7b-4ada-810c-e7234e4ed69d

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