FDA-Inspected Site

Spoonamore Drug Co Inc

2 FDA inspections are on record for Spoonamore Drug Co Inc in Louisville, United States.

483· Form 483 issued

Louisville, United States · Last updated July 9, 2026

Overview

  • 2 FDA inspections are on record.
  • 2 inspections produced a Form 483.
  • The most recent recorded inspection date is 2017-03-14.

At a glance

Inspections

2

Form 483s

2

EIRs

1

Last outcome

Form 483

Inspection history

FDA inspections on record, most recent first.

InspectionCategoryOutcomeForm 483
17 Jan 2017 – 14 Mar 2017Human Drugs483View 483 →
13 Jan 2015 – 3 Feb 2015Human DrugsWLOn file

Observations on record

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

14 Mar 2017
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Michael P Sheehan

14 Mar 2017
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Michael P Sheehan

14 Mar 2017
21 CFR 211.165(a)

Testing and release for distribution

Cited by Michael P Sheehan

14 Mar 2017
21 CFR 211.165(a)

Testing and release for distribution

Cited by Michael P Sheehan

14 Mar 2017
21 CFR 211.67(b)(6)

Cleaning SOP/inspection

Cited by Michael P Sheehan

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 211.113(b)Cited across public-safe Form 483 observations2x
21 CFR 211.165(a)Cited across public-safe Form 483 observations2x
21 CFR 211.67(b)(6)Cited across public-safe Form 483 observations2x

Full site report

Get the verbatim findings behind Spoonamore Drug Co Inc's 2 Form 483s

Source PDFs 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