FDA Inspection 1056097 — CLINLOGIX LLC

CLINLOGIX LLC — FEI 3012957356

The FDA completed an inspection of CLINLOGIX LLC on May 30, 2018 in Ambler, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 30, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Ambler, PA (United States)

Additional Details

Sponsor, Contract Research Organization