FDA Investigator Andrea S Heise
Andrea S Heise has conducted inspections on 6 sites in 1 countries as of 06 Jan 2021. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
6
Last Inspection Date:
06 Jan 2021
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 Andrea S Heise:
Alan P Kurtzberg,
Ana C Lazo,
Ana P Barido,
Andrew J Gonzales,
Barbara J Holladay,
Carlos Chavez,
Christopher M Jenner,
Deborah S Hammond,
Dongping Dai, PhD,
Dustin M James,
Edith M Gonzalez,
Erika V Butler,
Ginger M Sykes,
Haroon Vohra (NMI),
James D Bradley,
Jamie L Dion,
Joan M Cantellops Figueroa,
Kimberley A Hoefen,
La Tasham Gunter,
Laura L Staples,
Linda F Murphy,
Linda M Cheny,
Linda S Mattingly,
Margaret M Annes,
Marie B Buen Bigornia,
Marion W Nadeau,
Matthew R Dionne,
Michael A Charles,
Michael J Kuchta,
Michael R Goga,
Nancy L Meade,
Nayan J Patel,
Ricki A Chase,
Santos E Camara,
Sripal R Mada, PhD,
Stefanie R Cook,
Stephen T Hansen,
Teena H Aiken,
Terri L Thomas,
Theressa B Smith,
Uduak M Inokon,
Walden H Lee,
Yiyue Zhang (nmi), PhD,
Zachary A Bogorad,
Zachary L Miller,
Zachary L Stamm
Andrea S Heise's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2013 | FDA 483 | Front Range Laboratories, Inc. - Form 483, 2013-08-30 |
May, 2013 | FDA 483 | Corden Pharma Boulder, Inc. - Form 483, 2013-05-15 |
January, 2014 | FDA 483 | Actavis Laboratories UT, Inc. - Form 483, 2014-01-17 |
May, 2013 | EIR | Corden Pharma Boulder, Inc. - EIR, 2013-05-15 |
August, 2013 | FDA 483 | American National Red Cross - Form 483, 2013-08-30 |
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