FDA Inspection 1071342 — Henry Schein One LLC

Henry Schein One LLC — FEI 3013464458

The FDA completed an inspection of Henry Schein One LLC on Oct 26, 2018 in Ames, IA. 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
Oct 26, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Ames, IA (United States)

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