FDA-Inspected Site

QuantiPharm, Inc.

1 FDA inspection is on record for QuantiPharm, Inc. in Laval, Canada.

483· Form 483 issued

Laval, Canada · Last updated August 15, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2025-11-06.

At a glance

Inspections

1

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
4 Nov 2025 – 6 Nov 2025Human Drugs483View 483 →

Observations on record

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

6 Nov 2025
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Unnee Ranjan

6 Nov 2025
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Unnee Ranjan

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 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind QuantiPharm, Inc.'s 1 Form 483

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