FDA Investigator James D Romero
James D Romero has conducted inspections on 153 sites in 1 countries as of 18 Nov 2003. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
153
Last Inspection Date:
18 Nov 2003
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with James D Romero:
Andrea J Schmidt,
Andrew M Kolenc,
Antonetta M Colacchio,
Betty Kay Baxter,
Brandon K Lawson,
Brent W Higgs,
Brittany R Laymon,
Carla R Hinz,
Christine L Williams,
Daniel J Lahar,
Daniel Pst Laurent,
David A Gonzalez,
Debra L Curtis,
Denicia L Hernandez,
Dianna D Wardlow Dotter,
Donald R Hawn,
Edith M Gonzalez,
Elaine G Stewart,
Eric S Myskowski,
Erik W Burrows,
Felix J Marrero,
Frank L Cordova,
Gary C Pecic, Jr,
Gina M Scholze,
Ginger M Sykes,
Hanna L Potter,
Harry A Wilson,
Holly L Miller,
Isabel Y Espinosa,
Jamie L Dion,
Janet Pulver,
Jennifer A Baker,
Jennifer A Kinney,
Jennifer R Mathern,
Jessica M Ector,
Jessie E Morris,
Karen G Hirshfield,
Kathleen S Tormey,
Kathryn M Mogen,
Larry Gehring,
Laura B Kennedy,
Lavender M Huskey,
Linda F Murphy,
Linda M Cheny,
Manuel A Moreno,
Marc A Jackson, Jr,
Marie B Buen Bigornia,
Marion W Nadeau,
Marsha L Mccauley,
Martina E Lagrange,
Mary F Bodick,
Matthew A Johnson,
Matthew A Kozler,
Matthew R Dionne,
Melissa J Nucci,
Michael E Maselli,
Michael L Zimmerman,
Nancy G Schmidt,
Nathan M Jornod,
Nayan J Patel,
Oluwaseyi Ojinni,
Patricia A Maestas,
Paul J Teitell,
Philip E Ake,
Randy V Bong,
Richard T Jensen,
Russell R La Claire,
Sheila Alaghemand,
Shererk,
Solomon G Williams,
Steve P Yost,
Theressa B Smith,
Thomas V Anderson,
Trevor R Beach
James D Romero's Documents
Publish Date | Document Type | Title |
---|---|---|
November, 2000 | FDA 483 | Bud Shepherd & Sons Poultry Farm - Form 483, 2000-11-07 |
November, 2000 | EIR | Bud Shepherd & Sons Poultry Farm - EIR, 2000-11-07 |
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