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

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

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Record Summary

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

Violation Codes

21 CFR 820.180

21 CFR 820.198(c)

21 CFR 820.80(c)

21 CFR 820.90(b)(2)

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Record Information

Company

Oculus Surgical, Inc.

Inspection Date

February 27, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8eb3d0d-abd0-4ccb-85af-54e8ab575cc7

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