# Oculus Optikgeraete GMBH – FDA Inspection, Jun 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/oculus-optikgeraete-gmbh/aa16ecc0-8ad8-4caf-94aa-fe6de3a25e41
Source feed: FDA_Inspections

> FDA inspection 675579 of Oculus Optikgeraete GMBH, June 24, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 675579
- Company Name: Oculus Optikgeraete GMBH
- Inspection Date: 2010-06-24
- 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: 1

## Related Documents

- FDA Inspection 998293 - 2016-11-10
- FDA Inspection 853199 - 2013-09-19

Company: https://www.keypedia.com/companies/oculus-optikgeraete-gmbh/373f5590-2503-46cf-80fa-fe2b4ff19c85

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