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FDA Inspection 1022905 — Biotechne, Inc.

Biotechne, Inc. — FEI 1220649

The FDA completed an inspection of Biotechne, Inc. on July 20, 2017 in Devens, MA. 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
July 20, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Devens, MA (United States)

Facility

Other inspections at this facility

  • 819733 (NAI Wed Feb 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 703332 (NAI Thu Dec 23 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources