FDA Investigator Daniel L Obrzut
Daniel L Obrzut has conducted inspections on 5 sites in 5 countries as of 10 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
5
Last Inspection Date:
10 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
India,
Puerto Rico,
Italy,
Belgium,
United States of America
FDA Investigators that have inspected at least one site in common with Daniel L Obrzut:
Andrew J Barrowcliff,
Ariel Cruz Figueroa,
Arlene M Badillo,
Azza Talaat,
Bei Y He,
Brittany D Terhar,
Carla A Norris,
Charles R Cote, RIC,
Christopher R Czajka,
Constantin Y Philopoulos,
Courtney E Hillier,
Cynthia Jim, CSO,
Deborah A Greco,
Dennis Cantellops Paite,
Dr. Barbara D Paul, PhD,
Dr. Jason R Caballero,
Edwin Martinez,
Emilie E Kahn,
Emily J Orban,
German Rivera,
James C Maclaughlin,
Jeffrey D Meng,
Jeffrey P Raimondi,
Jorge L Guadalupe,
Jose A Lopez,
José E Meléndez,
Junho Pak,
Kathryn A Guardiola,
Kathryn G Brown,
Kejun Cheng,
Kellia N Hicks,
Kham Phommachanh,
Krishna Ghosh, PhD,
Kristy A Zielny,
Lareese K Thomas,
Lata C Mathew, PhD,
Lauren E Sexton,
Laurimer Kuilan Torres,
Libia M Lugo,
Lindsey S Fleischman,
Lisa J Joseph,
Lucas B Leake,
Marcus A Ray,
Marian E Ramirez,
Marianela Aponte Cruz,
Martin R Vowell,
Michele L Forster, PhD,
Muralidhara B Gavini, PhD,
Myriam M Sosa,
Nancy M Espinal,
Nina Ni,
Noreen Muñiz,
Patrick C Klotzbuecher,
Patsy J Domingo,
Ramon A Hernandez,
Rapti D Madurawe,
Raquel Gonzalez Rivera,
Rebecca E Dombrowski,
Rebecca Parrilla,
Rose Xu,
Ryan J Benedict,
Sanket N Patel,
Sarah E Rhoades,
Sarah M Meng,
Simone E Pitts,
Susan M Jackson,
Susan T Hadman,
Timothy T Kapsala,
Tracey L Harris,
Truong Xuan Nguyen (Andy),
Vilmary Negron Rodriguez,
Yifan Wang,
Ying Zhang
Daniel L Obrzut's Documents
Publish Date | Document Type | Title |
---|---|---|
May, 2018 | FDA 483 | Recipharm Pharmaservices Pvt. Ltd. - Form 483, 2018-05-11 |
February, 2024 | FDA 483 | Lilly del Caribe, Inc. - Form 483, 2024-02-16 |
December, 2019 | FDA 483 | Future Pak LLC - Form 483, 2019-12-12 |
June, 2024 | FDA 483 | NerPharMa S.r.l. - Form 483, 2024-06-19 |
June, 2024 | EIR | NerPharMa S.r.l. - EIR, 2024-07-15 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
![FDA Investigator Profile Icon](/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more