FDA Inspection 654252 — Techlab, Inc.

Techlab, Inc. — FEI 1000123404

The FDA completed an inspection of Techlab, Inc. on March 25, 2010 in Blacksburg, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 25, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Blacksburg, VA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation