Lenstec, Inc.

Form 483

St Petersburg, Florida, United StatesFEI 3001659659Issued July 18, 2013

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 3001659659.

Observations2

Issue DateJuly 18, 2013

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Lenstec, Inc.
Location: St Petersburg, Florida, United States
FEI Number: 3001659659
Product Type: Devices
Issue Date: July 18, 2013
Country: United States

Inspection History, 2012 to 2017

NAI2

VAI1

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Lenstec, Inc. FDA Form 483, St Petersburg, Florida, July 18, 2013