FDA Investigator Arthur T Ogdahl
Arthur T Ogdahl has inspections in 4 countries as of 13 Oct 2022. Arthur T Ogdahl has collaborated with a combinined 747 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
5
Last Inspection Date:
13 Oct 2022
Investigator Role:
FDA Investigator
Redica ID:
Country:
Austria,
Germany,
Belgium,
United States of America
Co-Investigator(s):
Andrew J Barrowcliff,
Anthony C Warchut,
Bonita S Chester,
Christina Capacci Daniel, PhD,
Christopher S Keating,
Denise M Digiulio,
Elvis D Morton,
Erika E Englund, PhD,
Felix Maldonado,
Jai P Singh,
James R Birkenstamm,
Jennifer J Stone,
Jessica D Nanini,
John D White,
John Dan,
Junho Pak,
Larry K Austin,
LCDR Debra Emerson,
Luella J Rossi,
Margaret M Annes,
Marvin D Jones,
Mary E Storch,
Matthew M Henciak,
Megan A Haggerty,
Michael A Charles,
Michael A Taylor,
Michael L Chasey,
Michelle E Noonan Smith,
Mildred L Mccray,
Mra Davism,
Myra L Reed,
Nebil A Oumer,
Robert C Steyert,
Roger F Zabinski,
Rose Xu,
State Agency,
Stephen J Koniers,
Steven M Weinman,
Tamara N Champion,
Temar Q Williams,
Teresa L Fox,
Thomas E Friel,
Zakaria I Ganiyu
Arthur T Ogdahl's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2000 | FDA 483 | Boehringer Ingelheim Pharma KG - Form 483, 2000-03-08 |
March, 2000 | FDA 483 Response | Boehringer Ingelheim Pharma GmbH and Co. KG - Form 483R, 2000-03-20 |
March, 2000 | FDA 483 Response | Patheon Austria GmbH & CoKG - Form 483R, 2000-05-30 |
March, 2000 | EIR | Boehringer Ingelheim Pharma GmbH and Co. KG - EIR, 2000-03-08 |
March, 2000 | EIR | Patheon Austria GmbH & CoKG - EIR, 2000-03-01 |
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