Form 483

Boehringer Ingelheim Pharma GmbH and Co. KG Form 483, 2019-04-05

FDA issued a Form 483 to Boehringer Ingelheim Pharma GmbH and Co. KG on 2019-04-05 with 2 public-safe observations.

483· Form 483 issuedHuman Drugs2 observations

Boehringer Ingelheim Pharma GmbH and Co. KG · Biberach An Der Ris, Germany · Issued April 5, 2019

Overview

  • 2 public-safe observations are available for this inspection.
  • 2 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.

5 Apr 2019
21 CFR 211.160(a)

Lab controls established, including changes

Cited by Doan T Nguyen, Doan N Singh

5 Apr 2019
21 CFR 211.192

Investigations of discrepancies, failures

Cited by Doan T Nguyen, Doan N Singh

Inspected site

BIBoehringer Ingelheim Pharma GmbH and Co. KGBiberach An Der Ris, Germany

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 observations1x
21 CFR 211.192Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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