FDA Inspection 1010179 — Techlab, Inc.

Techlab, Inc. — FEI 1000123404

The FDA completed an inspection of Techlab, Inc. on April 26, 2017 in Blacksburg, VA. 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 26, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Blacksburg, VA (United States)