FDA Inspection 824617 — Dukal Llc

Dukal Llc — FEI 1000137528

The FDA completed an inspection of Dukal Llc on March 20, 2013 in Ronkonkoma, NY. 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
March 20, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Ronkonkoma, NY (United States)