FDA Inspection 938613 — Hospitec Usa

Hospitec Usa — FEI 3008009298

The FDA completed an inspection of Hospitec Usa on Aug 17, 2015 in Fort Smith, AR. 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
Aug 17, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Smith, AR (United States)

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