Form 483

LEC Custom Products, Inc Form 483, 2019-09-12

FDA issued a Form 483 to LEC Custom Products, Inc on 2019-09-12 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

LEC Custom Products, Inc · Mississauga, Canada · Issued September 12, 2019

Overview

  • 6 public-safe observations are available for this inspection.
  • 6 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

12 Sep 2019
21 CFR 211.105(a)

Identification of containers, lines, equipment

Cited by Lauren N Howard

12 Sep 2019
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Lauren N Howard

12 Sep 2019
21 CFR 211.165(a)

Testing and release for distribution

Cited by Lauren N Howard

12 Sep 2019
21 CFR 211.188

Prepared for each batch, include complete information

Cited by Lauren N Howard

12 Sep 2019
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Lauren N Howard

Inspected site

LCLEC Custom Products, IncMississauga, Canada

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.105(a)Cited across public-safe Form 483 observations1x
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.165(a)Cited across public-safe Form 483 observations1x
21 CFR 211.188Cited across public-safe Form 483 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.22(d)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 6 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere