FDA-Inspected Site

NuTech Spine, Inc.

3 FDA inspections are on record for NuTech Spine, Inc. in Birmingham, United States.

483· Form 483 issued

Birmingham, United States · Last updated July 10, 2026

Overview

  • 3 FDA inspections are on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2019-06-20.

At a glance

Inspections

3

Form 483s

1

EIRs

0

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
18 Jun 2019 – 20 Jun 2019Medical Devices & Rad Health483View 483 →
13 Jul 2016Medical Devices & Rad HealthClean
16 Jun 2014 – 18 Jun 2014Medical Devices & Rad HealthClean

Observations on record

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

20 Jun 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Wendy R Blame

20 Jun 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Wendy R Blame

20 Jun 2019
21 CFR 820.100(a)

Lack of or inadequate procedures

Cited by Wendy R Blame

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 820.100(a)Cited across public-safe Form 483 observations3x

Full site report

Get the verbatim findings behind NuTech Spine, Inc.'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