FDA Inspection 1006644 — Symbio, LLC

Symbio, LLC — FEI 3009866066

The FDA completed an inspection of Symbio, LLC on Mar 16, 2017 in Port Jefferson, NY. 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
Mar 16, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Port Jefferson, NY (United States)

Additional Details

Sponsor, Contract Research Organization