FDA Inspection 717354 — Syntron Bioresearch Inc

Syntron Bioresearch Inc — FEI 2025760

The FDA completed an inspection of Syntron Bioresearch Inc on April 1, 2011 in Carlsbad, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Carlsbad, CA (United States)

Citations

IDCFRDescription
312121 CFR 820.80(b)Lack of or inadequate receiving acceptance procedures
312721 CFR 820.80(e)Documentation