FDA Inspection 1029549 — Cranial Solutions

Cranial Solutions — FEI 3003524425

The FDA completed an inspection of Cranial Solutions on September 25, 2017 in Pompton Lakes, NJ. 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 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Pompton Lakes, NJ (United States)