Form 483

Takeda Pharmaceutical Company Limited Form 483, 2013-09-06

FDA issued a Form 483 to Takeda Pharmaceutical Company Limited on 2013-09-06 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Takeda Pharmaceutical Company Limited · Yodogawa-Ku, Japan · Issued September 6, 2013

Overview

  • 5 public-safe observations are available for this inspection.
  • 5 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.

6 Sep 2013
21 CFR 211.22(d)

Procedures not in writing, fully followed

Cited by Nicholas A Violand, Xiaokuang Lai

6 Sep 2013
21 CFR 211.110(a)

Control procedures to monitor and validate performance

Cited by Nicholas A Violand, Xiaokuang Lai

6 Sep 2013
21 CFR 211.113(b)

Procedures for sterile drug products

Cited by Nicholas A Violand, Xiaokuang Lai

6 Sep 2013
21 CFR 211.165(e)

Test methods

Cited by Nicholas A Violand, Xiaokuang Lai

6 Sep 2013
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Nicholas A Violand, Xiaokuang Lai

Inspected site

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.110(a)Cited across public-safe Form 483 observations1x
21 CFR 211.113(b)Cited across public-safe Form 483 observations1x
21 CFR 211.165(e)Cited 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 5 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