FDA Inspection 871964 — Silgan Unicep Packaging, LLC

Silgan Unicep Packaging, LLC — FEI 1000150986

The FDA completed an inspection of Silgan Unicep Packaging, LLC on February 28, 2014 in Sandpoint, ID. 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
February 28, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Sandpoint, ID (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
323321 CFR 820.72(a)Calibration, Inspection, etc. Procedures Lack of or Inadequ