# CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC – FDA Inspection, Sep 15, 2017

Source: https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-cataract-technology-inc/d6b7382b-ed10-4e0c-9d27-e3b2436232dc
Source feed: FDA_Inspections

> FDA inspection 1025539 of CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC, September 15, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025539
- Company Name: CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC
- Inspection Date: 2017-09-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/carl-zeiss-meditec-cataract-technology-inc/5d69c901-9b57-4b98-a970-585d8abd5fde

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