Reproductive Gynecology Laboratories

Form 483

Akron, Ohio, United StatesFEI 3003928276Issued January 15, 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 3003928276.

Observations2

Issue DateJanuary 15, 2013

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: Reproductive Gynecology Laboratories
Location: Akron, Ohio, United States
FEI Number: 3003928276
Product Type: Biologics
Issue Date: January 15, 2013
Country: United States

Inspection History, 2011 to 2026

NAI6

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.

Reproductive Gynecology Laboratories FDA Form 483, Akron, Ohio, January 15, 2013