FDA Investigator: Laurimer Kuilan-Torres

- Laurimer Kuilan-Torres first started conducting FDA inspections in 2015, with the last inspection in 2024. Over that time, Laurimer Kuilan-Torres has conducted 70 inspections at 64 companies across 66 sites.

Get Laurimer Kuilan-Torres's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

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FDA 483 Baxter Pharmaceutical Solutions, LLC, Bloomington | 2024

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Laurimer Kuilan-Torres
Human Drugs Form 483

FDA 483 FUJIFILM Diosynth Biotechnologies Texas, LLC, College Station | 2023

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Laurimer Kuilan-Torres
Human Drugs Form 483

FDA 483 Takeda Pharmaceutical Company Limited, Hikari | 2023

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Laurimer Kuilan-Torres
Human Drugs Form 483

FDA 483 Ajinomoto Althea, Inc., San Diego | 2023

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Laurimer Kuilan-Torres
Human Drugs Form 483

FDA 483 Kashiv BioSciences, LLC, Chicago | 2022

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Laurimer Kuilan-Torres
Human Drugs Form 483

FDA 483 Yabao Pharmaceutical Co., Ltd. Beijing, Beijing | 2022

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Laurimer Kuilan-Torres
Human Drug Form 483

FDA 483 Jiangxi Aifeimu Technology Co., Ltd., Wannian City | 2019

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Laurimer Kuilan-Torres
Human Drug Form 483

FDA 483 Zhejiang Regen Chemical Co., Ltd., Taizhou | 2019

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Laurimer Kuilan-Torres
Human Drug Form 483

FDA 483 Jiangsu Province Jianerkang Medical Dressing Co., Ltd, Changzhou | 2019

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Laurimer Kuilan-Torres
Human Drug Form 483