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FDA Inspection
•Boehringer Ingelheim Fremont, Inc.•April 4, 2017

Boehringer Ingelheim Fremont, Inc. – FDA Inspection, Apr 4, 2017

Record Details

This FDA Inspection record concerns Boehringer Ingelheim Fremont, Inc., with an inspection on April 4, 2017, issued by the San Francisco District Office, covering human drugs.

Company
Boehringer Ingelheim Fremont, Inc.
Inspection Date
April 4, 2017
Product Type
Human Drugs
Office
San Francisco District Office
People
  • Diane L. Raccasi (Issuing Officer)
  • Ephrem T. Hunde (Issuing Officer)
  • Kristin M. Abaonza (FDA Associated Person)
  • Maria I. Cruz-Fisher (Issuing Officer)
  • Monica M. Commerford (Issuing Officer)
View Company Profile

ID · ff7cd87f-90a8-4b66-8652-6004f0512e9e

Inspection Facts

Inspection number
1005958
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Boehringer Ingelheim Fremont, Inc.

7
DateClassificationOfficeProject area
May 16, 2024Not classifiedSan Francisco District Office
April 13, 2023Not classifiedSan Francisco District Office
November 4, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 24, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 28, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Boehringer Ingelheim Fremont, Inc.
  • FDA Inspection 1263388 - 2024-05-16
  • FDA Inspection 1205076 - 2023-04-13
  • FDA Inspection 1187410 - 2022-11-04
  • FDA Inspection 1063730 - 2018-08-24
  • FDA Inspection 882791 - 2014-05-28

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