Form 483

Winder Laboratories, LLC Form 483, 2020-03-13

FDA issued a Form 483 to Winder Laboratories, LLC on 2020-03-13 with 4 public-safe observations.

483· Form 483 issuedHuman Drugs4 observations

Winder Laboratories, LLC · Winder, United States · Issued March 13, 2020

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 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.

13 Mar 2020
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Susan O Oladeji

13 Mar 2020
21 CFR 211.198(b)(3)

Reason for Not Conducting Complaint Investigation

Cited by Susan O Oladeji

13 Mar 2020
21 CFR 211.63

Equipment Design, Size and Location

Cited by Susan O Oladeji

13 Mar 2020
21 CFR 211.84(d)(6)

Objectionable microbiological contamination

Cited by Susan O Oladeji

Inspected site

WLWinder Laboratories, LLCWinder, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.192Cited across public-safe Form 483 observations1x
21 CFR 211.198(b)(3)Cited across public-safe Form 483 observations1x
21 CFR 211.63Cited across public-safe Form 483 observations1x
21 CFR 211.84(d)(6)Cited across public-safe Form 483 observations1x

Source document

PDF
PDF available

Form 483 source document

The source document is available to authorized Atlas users.

Full 483 report

Get the verbatim text of all 4 observations

The source PDF, 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