Danmar Products, Inc.

Form 483

Ann Arbor, Michigan, United StatesFEI 1831680Issued October 30, 2014

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 1831680.

Observations2

Issue DateOctober 30, 2014

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Danmar Products, Inc.
Location: Ann Arbor, Michigan, United States
FEI Number: 1831680
Product Type: Devices
Issue Date: October 30, 2014
Country: United States

Inspection History, 2009 to 2024

NAI1

VAI4

OAI1

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

Danmar Products, Inc. FDA Form 483, Ann Arbor, Michigan, October 30, 2014