FDA Inspection 699599 — Sterigenics Belgium Petit-Rechain S.A.

Sterigenics Belgium Petit-Rechain S.A. — FEI 3002807111

The FDA completed an inspection of Sterigenics Belgium Petit-Rechain S.A. on Nov 11, 2010 in Verviers. 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
Nov 11, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Verviers (Belgium)

Additional details

Postmarket Audit Inspections

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