Frontida BioPharm Inc

Form 483

Philadelphia, Pennsylvania, United StatesFEI 2523348Issued July 17, 2015

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 2523348.

Observations10

Issue DateJuly 17, 2015

StatusNo Warning Letter

Related Inspections10

Establishment Details

Firm: Frontida BioPharm Inc
Location: Philadelphia, Pennsylvania, United States
FEI Number: 2523348
Product Type: Drugs
Issue Date: July 17, 2015
Country: United States

Inspection History, 2009 to 2026

NAI3

VAI6

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.

Frontida BioPharm Inc FDA Form 483, Philadelphia, Pennsylvania, July 17, 2015