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FDA Inspection 1014496 — Silgan Unicep Packaging, LLC

Silgan Unicep Packaging, LLC — FEI 1000150986

The FDA completed an inspection of Silgan Unicep Packaging, LLC on March 30, 2017 in Sandpoint, ID. 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
March 30, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sandpoint, ID (United States)

Facility

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  • 1053505 (VAI Fri May 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 991913 (VAI Fri Nov 04 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871964 (VAI Fri Feb 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 845770 (NAI Wed Aug 07 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources