Huntington Reproductive Center Medical Group

Form 483FOIA Uncovered

Newport Beach, California, United StatesFEI 3009565053Issued March 28, 2023

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 3009565053.

Observations2

Issue DateMarch 28, 2023

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Huntington Reproductive Center Medical Group
Location: Newport Beach, California, United States
FEI Number: 3009565053
Product Type: Biologics
Issue Date: March 28, 2023
Country: United States

Inspection History, 2015 to 2024

NAI3

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.

Huntington Reproductive Center Medical Group FDA Form 483, Newport Beach, California, March 28, 2023