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FDA Inspection 830015 — Lacrimedics Inc

Lacrimedics Inc — FEI 2024818

The FDA completed an inspection of Lacrimedics Inc on April 26, 2013 in Dupont, WA. 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
April 26, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dupont, WA (United States)

Facility

Other inspections at this facility

  • 1115703 (NAI Thu Jan 23 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 966842 (NAI Tue Mar 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 731251 (NAI Thu Jun 23 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 588516 (NAI Tue Jun 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources