FDA Inspection 573253 — AMO Uppsala AB

AMO Uppsala AB — FEI 3004750704

The FDA completed an inspection of AMO Uppsala AB on Mar 19, 2009 in Uppsala. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Mar 19, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Uppsala (Sweden)

Additional details

Postmarket Audit Inspections

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