FDA Inspection 647943 — SEDECAL SA

SEDECAL SA — FEI 3002495042

The FDA completed an inspection of SEDECAL SA on Jan 15, 2010 in Algete. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 15, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Algete (Spain)

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