FDA Inspection 842806 — Arjo Inc.

Arjo Inc. — FEI 3009988881

The FDA completed an inspection of Arjo Inc. on August 2, 2013 in San Antonio, TX. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Antonio, TX (United States)

Citations

IDCFRDescription
317021 CFR 820.198(b)Review and evaluation for investigation