Form 483

Fresenius USA Manufacturing, Inc Form 483, 2017-10-06

FDA issued a Form 483 to Fresenius USA Manufacturing, Inc on 2017-10-06 with 2 public-safe observations.

483· Form 483 issuedHuman Drugs2 observations

Fresenius USA Manufacturing, Inc · Knoxville, United States · Issued October 6, 2017

Overview

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

Inspectional observations

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

6 Oct 2017
21 CFR 211.160(a)

Deviations from laboratory control requirements

Cited by Brandon C Heitmeier

6 Oct 2017
21 CFR 211.160(a)

Deviations from laboratory control requirements

Cited by Brandon C Heitmeier

Inspected site

FUFresenius USA Manufacturing, IncKnoxville, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

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

Full 483 report

Get the verbatim text of all 2 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