FDA Inspection 821225 — Allerderm Laboratories Inc

Allerderm Laboratories Inc — FEI 2918720

The FDA completed an inspection of Allerderm Laboratories Inc on February 6, 2013 in Phoenix, AZ. 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 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)