Gilead Sciences, Inc.

FDA inspection history in La Verne, California, 2021 to 2026

5
Form 483s

Every document, by year

  • Form 483

2021: one Form 483; 2022: one Form 483; 2024: one Form 483; 2026: two Form 483s.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2021–26Five Form 483s, at La Verne, California.
  2. 2026The longest 483 on file: 7 observations over 10 pages at La Verne, California.

Cited most

Across all Gilead Sciences observations on file

The complete Gilead Sciences file.

All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

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Sites

Documents

5 on file, newest first
DateDocumentPrice
2026-02-18483 Form 483$99
2026-02-09483 Form 483$99
2024-02-12483 Form 483$99
2022-09-16483 Form 483$99
2021-12-17483 Form 483$99

FEI number 3013189568 · most recent document Feb 18, 2026

About Gilead Sciences, Inc.

How many FDA Form 483s has Gilead Sciences, Inc. received?

FDA Intel has 5 Form 483s on file for Gilead Sciences, Inc.; the most recent is dated Feb 18, 2026.

When was Gilead Sciences, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Gilead Sciences, Inc. is a Form 483 dated Feb 18, 2026, for the site in La Verne, California.

What did FDA cite at Gilead Sciences, Inc.?

The regulations cited most in the observations on file for Gilead Sciences, Inc. are 21 CFR 211.160 (General requirements), 5 times; 21 CFR 211.170(b) (Reserve samples), 4 times; 21 CFR 211.113(b) (Control of microbiological contamination), 3 times.

Gilead Sciences, Inc. FDA Inspection History & 483s · FDA Intel