# FDA Inspection 1025539 - CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC - September 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 for CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC on September 15, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025539 - 2017-09-15](https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-cataract-technology-inc/170a6ad9-ad3e-4a09-87f4-f4e9386cbb06)

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