FDA Investigator Heather A Mccauley
Heather A Mccauley has conducted inspections on 6 sites in 1 countries as of 27 Feb 2023. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
6
Last Inspection Date:
27 Feb 2023
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 Heather A Mccauley:
Alan Escalona,
Alec M O'neal,
Allison M Scheck,
Andrew I Carr,
Andrew M Kupper,
Anna M Brannen,
Arie R Dyk,
Ariel J Cutchins,
Bailey A Uetrecht,
Benjamin P Stewart,
Brenda C Hamilton,
Brian L Boyd,
Brittany M Kershaw,
Carlos H Ruiz,
Catherine D Djordjevic,
Christina L Bigham,
Christopher D Snyder,
Craig P Seaborn,
Cynthia T Cain,
Darren S Morgan,
David P Moorhead,
Donna F Campbell,
Edward R Kay,
Elizabeth Ll Edwards,
Elizabeth P Kinsella,
Evan M Kupper,
Holly J Rapier,
Holly J Wilson,
James G Marsh,
Jason Channels,
Jason D Werne,
Javonica F Penn,
Jennifer L Gustavus,
John P Roetting, II,
Jon P Antoniou,
Joshua S Hunt,
Kathryn Carroll,
Katie L Korchinski,
Keith J Mason, Jr,
Kenneth E Felkley,
Kimberly A Joseph,
Lauren N Howard,
Lauren N Smith,
Lindsey M Schwierjohann,
Lisa R Hilliar,
Maney P Sturgill,
Marianne Allen,
Maribeth G Niesen,
Mark E Parmon,
Matt D Suedkamp,
Michael D Thatcher,
Michael P Sheehan,
Nadeem I Chaudhry,
Nicholas L Paulin,
Philip S Woodward,
Pifer,
Raquel L Coleman,
Richard W Berning,
Robbie J Alleman,
Roy C Stephens,
Steven P Eastham,
Susan M Taylor,
Talmane J Fisher,
Tamara M Kays,
Teresa K Kastner,
Thomas J Prigge,
Tracey L Harris,
Wen Ning Chan (Sally),
Yvette Mlacour Davis
Heather A Mccauley's Documents
Publish Date | Document Type | Title |
---|---|---|
February, 2016 | EIR | Dole Fresh Vegetables, Inc. - EIR, 2016-02-05 |
May, 2017 | EIR | Adare Pharmaceuticals, Inc. - EIR, 2017-05-19 |
February, 2016 | FDA 483 | Dole Fresh Vegetables, Inc. - Form 483, 2016-02-05 |
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