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FDA Inspection 679573 — Ethicon Endo-Surgery Inc

Ethicon Endo-Surgery Inc — FEI 1527736

The FDA completed an inspection of Ethicon Endo-Surgery Inc on August 19, 2010 in Blue Ash, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Blue Ash, OH (United States)

Facility

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FDA data resources