Midwest Fertility Specialists

Form 483

Carmel, Indiana, United StatesFEI 3005620323Issued January 31, 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 3005620323.

Observations4

Issue DateJanuary 31, 2013

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Midwest Fertility Specialists
Location: Carmel, Indiana, United States
FEI Number: 3005620323
Product Type: Biologics
Issue Date: January 31, 2013
Country: United States

Inspection History, 2010 to 2024

NAI4

VAI2

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.

Midwest Fertility Specialists FDA Form 483, Carmel, Indiana, January 31, 2013