FDA-Inspected Site

Frontida BioPharm Inc

21 FDA inspections are on record for Frontida BioPharm Inc in Philadelphia, United States.

Clean· No action indicated

Philadelphia, United States · Last updated July 9, 2026

Overview

  • 21 FDA inspections are on record.
  • 7 inspections produced a Form 483.
  • The most recent recorded inspection date is 2026-04-02.

At a glance

Inspections

21

Form 483s

7

EIRs

1

Last outcome

Clean

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
30 Mar 2026 – 2 Apr 2026Human DrugsClean
21 Jul 2025 – 22 Jul 2025Tobacco ProductsClean
28 Nov 2023 – 7 Dec 2023Human Drugs483View 483 →
15 Jul 2019 – 19 Jul 2019Human Drugs483View 483 →
12 Jul 2017 – 20 Jul 2017Human DrugsClean
16 Mar 2017 – 31 Mar 2017Human Drugs483View 483 →
15 Jun 2015 – 17 Jul 2015Human DrugsWLView 483 →
30 Jun 2014 – 25 Jul 2014Human Drugs483View 483 →
27 Jan 2012Not recorded483On file
20 May 2011Not recorded483View 483 →
30 Jun 2009Not recordedClean
10 Dec 2008Not recordedClean

Observations on record

Form 483 observations cited at this site, most recent first.

7 Dec 2023
21 CFR 211.67(a)

Cleaning / Sanitizing / Maintenance

Cited by Anastasia M Shields

7 Dec 2023
21 CFR 211.67(a)

Cleaning / Sanitizing / Maintenance

Cited by Anastasia M Shields

7 Dec 2023
21 CFR 314.81(b)(1)(ii)

Contamination, chemical or physical change, deterioration

Cited by Anastasia M Shields

7 Dec 2023
21 CFR 314.81(b)(1)(ii)

Contamination, chemical or physical change, deterioration

Cited by Anastasia M Shields

19 Jul 2019
21 CFR 211.194(a)

Complete test data included in records

Cited by Michael L Casner, Jaison J Eapen

Investigators

FDA investigators tied to this site in the record.

Recurring citations

CFR citation patterns observed across this site's inspections.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations6x
21 CFR 314.81(b)(1)(ii)Cited across public-safe Form 483 observations4x
21 CFR 211.100(a)Cited across public-safe Form 483 observations2x
21 CFR 211.100(b)Cited across public-safe Form 483 observations2x
21 CFR 211.67(a)Cited across public-safe Form 483 observations2x
21 CFR 211.110(b)Cited across public-safe Form 483 observations1x
21 CFR 211.111Cited across public-safe Form 483 observations1x
21 CFR 211.150(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.160(b)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.165(f)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)Cited across public-safe Form 483 observations1x
21 CFR 211.166(a)(4)Cited across public-safe Form 483 observations1x
21 CFR 211.186(a)Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)Cited across public-safe Form 483 observations1x
21 CFR 211.194(a)(1)Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x
21 CFR 211.67(b)Cited across public-safe Form 483 observations1x
21 CFR 314.81(b)(1)(i)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Frontida BioPharm Inc's 7 Form 483s

Source PDFs, verbatim observations, and recurring CFR citations, so your team knows what this site gets cited for.

  • The site's full inspection history, with every Form 483 and its outcome
  • Warning letters and recalls tied to the company behind it
  • Whether recurring CFR citations get closed out or repeat