FDA Inspection 701444 — G. Dundas Co Inc

G. Dundas Co Inc — FEI 3019855

The FDA completed an inspection of G. Dundas Co Inc on November 8, 2010 in Black Diamond, WA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 8, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Black Diamond, WA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ
333121 CFR 820.181DMR - not or inadequately maintained
383721 CFR 820.25(b)Training records
41921 CFR 820.20(b)Lack of or inadequate organizational structure