FDA-Inspected Site

Blendpack Inc

1 FDA inspection is on record for Blendpack Inc in Cleveland, United States.

483· Form 483 issued

Cleveland, United States · Last updated July 12, 2026

Overview

  • 1 FDA inspection is on record.
  • 1 inspection produced a Form 483.
  • The most recent recorded inspection date is 2024-11-01.

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
28 Oct 2024 – 1 Nov 2024Animal Drugs & Feeds483View 483 →

Observations on record

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

1 Nov 2024
21 CFR 211.113(a)

Procedures for non-sterile drug products

Cited by Gretchen M Laws, Inga M Warr

1 Nov 2024
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Gretchen M Laws, Inga M Warr

1 Nov 2024
21 CFR 211.63

Equipment Design, Size and Location

Cited by Gretchen M Laws, Inga M Warr

1 Nov 2024
21 CFR 211.84(d)(2)

Component identification test

Cited by Gretchen M Laws, Inga M Warr

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(a)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 211.84(d)(2)Cited across public-safe Form 483 observations1x

Full site report

Get the verbatim findings behind Blendpack Inc's 1 Form 483

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