FDA Inspection 927509 — Arjo Inc.

Arjo Inc. — FEI 3009988881

The FDA completed an inspection of Arjo Inc. on May 19, 2015 in San Antonio, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Antonio, TX (United States)