FDA Inspection 607471 — Phase I Corp.

Phase I Corp. — FEI 1000305593

The FDA completed an inspection of Phase I Corp. on Mar 25, 2009 in Danbury, CT. 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 25, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Danbury, CT (United States)