FDA Inspection 636985 — Arrow International, Inc. (subsidiary of Teleflex, Inc.)

Arrow International, Inc. (subsidiary of Teleflex, Inc.) — FEI 3010532612

The FDA completed an inspection of Arrow International, Inc. (subsidiary of Teleflex, Inc.) on January 22, 2010 in Chelmsford, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Chelmsford, MA (United States)

Citations

IDCFRDescription
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures