FDA Inspection 1040314 — Steribite, LLC

Steribite, LLC — FEI 3009662229

The FDA completed an inspection of Steribite, LLC on Dec 21, 2017 in Wooster, OH. 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
Dec 21, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Wooster, OH (United States)

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