Dentium USA

Form 483

Cypress, California, United StatesFEI 3005503242Issued July 21, 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 3005503242.

Observations4

Issue DateJuly 21, 2009

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Dentium USA
Location: Cypress, California, United States
FEI Number: 3005503242
Product Type: Devices
Issue Date: July 21, 2009
Country: United States

Inspection History, 2009 to 2018

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.

Dentium USA FDA Form 483, Cypress, California, July 21, 2009