Form 483

Astellas Pharma Inc. Form 483, 2018-03-02

FDA issued a Form 483 to Astellas Pharma Inc. on 2018-03-02 with 6 public-safe observations.

483· Form 483 issuedHuman Drugs6 observations

Astellas Pharma Inc. · Toyama, Japan · Issued March 2, 2018

Overview

  • 6 public-safe observations are available for this inspection.
  • 3 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.

2 Mar 2018
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Saied A Asbagh

2 Mar 2018
21 CFR 211.188

Prepared for each batch, include complete information

Cited by Saied A Asbagh

2 Mar 2018
21 CFR 820.75(a)

Documentation

Cited by Saied A Asbagh

2 Mar 2018
21 CFR 211.160(b)

Scientifically sound laboratory controls

Cited by Saied A Asbagh

2 Mar 2018
21 CFR 211.188

Prepared for each batch, include complete information

Cited by Saied A Asbagh

Inspected site

APAstellas Pharma Inc.Toyama, Japan

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 211.160(b)Cited across public-safe Form 483 observations2x
21 CFR 211.188Cited across public-safe Form 483 observations2x
21 CFR 820.75(a)Cited across public-safe Form 483 observations2x

Full 483 report

Get the verbatim text of all 6 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