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FDA Inspection 1019242 — Karl Storz Imaging Inc.

Karl Storz Imaging Inc. — FEI 2027009

The FDA completed an inspection of Karl Storz Imaging Inc. on June 22, 2017 in Goleta, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Goleta, CA (United States)

Facility

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FDA data resources