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FDA Inspection
•Gene Logic, Inc.•February 21, 2018

Gene Logic, Inc. – FDA Inspection, Feb 21, 2018

Record Details

This FDA Inspection record concerns Gene Logic, Inc., with an inspection on February 21, 2018, issued by the Baltimore District Office, covering animal drugs & feeds.

Company
Gene Logic, Inc.
Inspection Date
February 21, 2018
Product Type
Animal Drugs & Feeds
Office
Baltimore District Office
People
  • Courtney N. Long (Company Rep)
  • David L. Chon (Investigator)
View Company Profile

ID · cfc7b4b8-2c34-4ac6-bd9f-28720023a445

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1042542
FDA center
Animal Drugs & Feeds
Project area
Pre-Approval Eval. of Animal Drugs and Food Additives
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 58.90(d)Animal care: animal identification

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Gene Logic, Inc.

4
DateClassificationOfficeProject area
March 18, 2025Not classifiedBaltimore District Office
March 29, 2024Not classifiedBaltimore District Office
March 1, 2023Not classifiedBaltimore District Office
March 22, 2019Not classifiedBaltimore District Office
Other documents for Gene Logic, Inc.
  • FDA Inspection 1266356 - 2025-03-18
  • FDA Inspection 1237219 - 2024-03-29
  • FDA Inspection 1201727 - 2023-03-01
  • FDA Inspection 1102011 - 2019-03-22

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