Lacrimedics Inc

Form 483

Dupont, Washington, United StatesFEI 2024818Issued June 09, 2009

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2024818.

Observations2

Issue DateJune 09, 2009

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Lacrimedics Inc
Location: Dupont, Washington, United States
FEI Number: 2024818
Product Type: Devices
Issue Date: June 09, 2009
Country: United States

Inspection History, 2009 to 2020

NAI2

VAI3

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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Lacrimedics Inc FDA Form 483, Dupont, Washington, June 9, 2009