FDA Inspection 571611 — Limerick Inc

Limerick Inc — FEI 3002297831

The FDA completed an inspection of Limerick Inc on February 25, 2009 in Burbank, CA. 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
February 25, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Burbank, CA (United States)