# FDA Inspection 853199 - Oculus Optikgeraete GMBH - September 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/oculus-optikgeraete-gmbh/2c91d67c-d92e-4f09-a1ae-1be90c1f51a8
Source feed: FDA_Inspections

> FDA Inspection 853199 for Oculus Optikgeraete GMBH on September 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 853199
- Company Name: Oculus Optikgeraete GMBH
- Inspection Date: 2013-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 853199 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/oculus-optikgeraete-gmbh/2d02258b-6402-480b-9cf2-26a9aa4cc82d)
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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