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FDA Inspection 731251 — Lacrimedics Inc

Lacrimedics Inc — FEI 2024818

The FDA completed an inspection of Lacrimedics Inc on June 23, 2011 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
June 23, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: 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))
  • 830015 (NAI Fri Apr 26 2013 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