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FDA Inspection 633629 — Merz North America, Inc.

Merz North America, Inc. — FEI 1012187

The FDA completed an inspection of Merz North America, Inc. on November 24, 2009 in Raleigh, NC. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 24, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Raleigh, NC (United States)

Facility

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