FDA Investigator Krystyna M Kitson
Krystyna M Kitson has conducted inspections on 8 sites in 1 countries as of 01 Jul 2009. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
8
Last Inspection Date:
01 Jul 2009
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 Krystyna M Kitson:
Amy M Cramer,
Annemarie Bodnar,
Antoinette L Ravelli,
Azeezat M Lawal,
Barbara Jwilimczyk Macri,
Bing Lin,
Carol A Perry,
Christian F Gomez Lugo,
Christina K Theodorou,
Christopher J Hurst,
Daniel J Grabicki,
David A Oluwo,
Devon Jenkins,
Gillian B Nardelli,
Janaye A Young,
Jo Annc Declement,
Jonathan G Matrisciano,
Jose M Cayuela,
Joy Rkozlowski Klena,
Judith A Jones,
Judith A Paterson,
Justine Tomasso,
Karen E D'orazio,
Karen F Tomaziefski,
Keith A Schwartz,
Kyle D Covill,
Lauren L Vajo,
Lisa Harlan,
Loretta Nemchik,
Lori M Newman,
Marcelo O Mangalindan, Jr,
Marea K Harmon,
Margaret M Sands,
Matthew S Mccollough,
Meredith L Sheridan,
Michael Rosner,
Nancy M Espinal,
Nicholas A Violand,
Paul L Bellamy,
Ramanda C Gregory,
Raymond L Cheung,
Regina T Brown,
Robert W Calais,
Rochelle L Cross,
Ronald T Colucci,
Rosario D'costa,
Russell J Glapion,
Sean R Marcsisin,
Seng Ching Hwang,
Tamil Arasu, PhD,
Teigan M Mule,
William J Muszynski,
William W Dotts,
Yoriann M Cabrera Bartolomei,
Yvesna C Blaise
Krystyna M Kitson's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2009 | FDA 483 | H & P Industries, Inc. - Form 483, 2009-03-12 |
April, 2009 | FDA 483 | Akers Biosciences, Inc. - Form 483, 2009-04-09 |
March, 2009 | FDA 483 | Hikma Pharmaceuticals USA Inc. - Form 483, 2009-03-10 |
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