FDA Investigator Lesley Maep Lutao

Lesley Maep Lutao has conducted inspections on 42 sites in 1 countries as of 03 Jun 2024. See below for a list of the FDA enforcement documents resulting from those inspections.

Investigator Details

Number of Inspected Sites:
42
Last Inspection Date:
03 Jun 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America

Lesley Maep Lutao's Documents

Publish Date Document Type Title
February, 2024 FDA 483 Indiana Lions Eye Bank, Inc. (dbA VisionFirst Indiana Lions Eye Bank) - Form 483, 2024-02-05
October, 2023 FDA 483 Institute for Human Reproduction (IHR), SC - Form 483, 2023-10-25
August, 2023 FDA 483 GPI USA, Inc. - Form 483, 2023-08-25
January, 2023 FDA 483 Reproductive Services Of Indiana, Inc - Form 483, 2023-01-20
November, 2023 FDA 483 Family Beginnings, PC - Form 483, 2023-11-20
January, 2024 FDA 483 Community Fertility Specialty Care - Form 483, 2024-01-11
June, 2023 FDA 483 BHC, LLC - Form 483, 2023-06-30
October, 2023 FDA 483 Fertility Centers of Illinois - Form 483, 2023-10-18
July, 2024 FDA 483 Healthcare-id, Inc. - Form 483, 2024-07-18
June, 2024 FDA 483 Cryomate Indiana LLC - Form 483, 2024-06-07
May, 2024 FDA 483 Ossium Health, Inc. - Form 483, 2024-05-30
September, 2024 FDA 483 Versiti Indiana Inc - Form 483, 2024-09-30
December, 2024 FDA 483 Biomat USA, Inc. - Form 483, 2024-12-13
February, 2025 FDA 483 Veterans Affairs Palo Alto Health Care System - Form 483, 2025-02-13
February, 2025 FDA 483 Reproductive Science Center of the San Francisco Bay Area, a Medical Corporation - Form 483, 2025-02-05
November, 2024 FDA 483 Midwest Fertility Specialists - Form 483, 2024-11-25
April, 2025 FDA 483 Department of Defense - Navy (U.S. Naval Hospital Naples) - Form 483, 2025-04-15
May, 2025 FDA 483 Lattice Inc - Form 483, 2025-05-22
December, 2024 FDA 483 Octapharma Plasma, Inc. - Form 483, 2024-12-20
December, 2025 FDA 483 KEDPLASMA LLC - Form 483, 2025-12-16
July, 2025 FDA 483 Eurofins Donor & Product Testing, LLC, San Ramon - Form 483, 2025-07-18
January, 2026 FDA 483 Life Line Stem Cell, Inc. - Form 483, 2026-01-16

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