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FDA Inspection 778684 — Cranial Solutions

Cranial Solutions — FEI 3003524425

The FDA completed an inspection of Cranial Solutions on April 20, 2012 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
April 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Pompton Lakes, NJ (United States)

Facility

Other inspections at this facility

  • 1029549 (NAI Mon Sep 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 709427 (OAI Fri Jan 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 662534 (OAI Fri May 14 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources