FDA Inspection 747292 — InterCare DX, Inc

InterCare DX, Inc — FEI 3005735282

The FDA completed an inspection of InterCare DX, Inc on September 27, 2011 in Torrance, 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
September 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Torrance, CA (United States)