FDA-Inspected Site

NEOTRON SPA

2 FDA inspections are on record for NEOTRON SPA in Modena, Italy.

483· Form 483 issued

Modena, Italy · Last updated July 10, 2026

Overview

  • 2 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2019-09-06.

At a glance

Inspections

2

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
5 Sep 2019 – 6 Sep 2019Human Drugs483View 483 →
6 Jul 2017 – 7 Jul 2017Human DrugsClean

Observations on record

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

6 Sep 2019
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Jose A Cruz Gonzalez

6 Sep 2019
21 CFR 211.192

Extent of discrepancy, failure investigations

Cited by Jose A Cruz Gonzalez

6 Sep 2019
21 CFR 211.192

Quality control unit review of records

Cited by Jose A Cruz Gonzalez

6 Sep 2019
21 CFR 211.68(a)

Calibration/Inspection/Checking not done

Cited by Jose A Cruz Gonzalez

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 observations2x
21 CFR 211.160(b)Cited across public-safe Form 483 observations1x
21 CFR 211.68(a)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind NEOTRON SPA's 1 Form 483

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