FDA Inspection 694703 — American Catheter Corp

American Catheter Corp — FEI 1000151187

The FDA completed an inspection of American Catheter Corp on October 21, 2010 in Jupiter, FL. 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
October 21, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jupiter, FL (United States)