# FDA Inspection 916800 - Oculus Surgical, Inc. - February 27, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/oculus-surgical-inc/f8eb3d0d-abd0-4ccb-85af-54e8ab575cc7/
Source feed: FDA_Inspections

> FDA Inspection 916800 for Oculus Surgical, Inc. on February 27, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916800
- Company Name: Oculus Surgical, Inc.
- Inspection Date: 2015-02-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/oculus-surgical-inc/02bec6cc-18ae-46ce-b2a7-65c3e0d83472

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