Form 483

WES Pharma Inc. Form 483, 2019-12-20

FDA issued a Form 483 to WES Pharma Inc. on 2019-12-20 with 8 public-safe observations.

483· Form 483 issuedHuman Drugs8 observations

WES Pharma Inc. · Westminster, United States · Issued December 20, 2019

Overview

  • 8 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 2 investigators are tied to this Form 483.

Inspectional observations

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

20 Dec 2019
21 CFR 211.166(a)(2)

Stability sample storage conditions described

Cited by David A Oluwo, Anitha P Govada

20 Dec 2019
21 CFR 211.166(a)(2)

Stability sample storage conditions described

Cited by David A Oluwo, Anitha P Govada

20 Dec 2019
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by David A Oluwo, Anitha P Govada

20 Dec 2019
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by David A Oluwo, Anitha P Govada

20 Dec 2019
21 CFR 211.63

Equipment Design, Size and Location

Cited by David A Oluwo, Anitha P Govada

Inspected site

WPWES Pharma Inc.Westminster, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.166(a)(2)Cited across public-safe Form 483 observations2x
21 CFR 211.22(d)Cited across public-safe Form 483 observations2x
21 CFR 211.63Cited across public-safe Form 483 observations2x
21 CFR 211.67(b)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 8 observations

The full inspection record, as Atlas holds it, 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