FDA Inspection 817224 — 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 Feb 6, 2013 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
Feb 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Verviers (Belgium)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.