Genentech, Inc.
FDA inspection history in Oceanside, California, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Oceanside, California.
Cited most
Across all Genentech observations on file
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.58Maintenance1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Genentech file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Oceanside, California
One Form 483 · 2017 · 2 observations
Latest: Form 483, Oct 18, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-10-18 | 483 Form 483 | Oceanside, California | 2 | $99 |
Investigators on these documents
FEI number 3006129086 · most recent document Oct 18, 2017
About Genentech, Inc.
How many FDA Form 483s has Genentech, Inc. received?
FDA Intel has 1 Form 483 on file for Genentech, Inc.; the most recent is dated Oct 18, 2017.
When was Genentech, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Genentech, Inc. is a Form 483 dated Oct 18, 2017, for the site in Oceanside, California.
What did FDA cite at Genentech, Inc.?
The regulations cited most in the observations on file for Genentech, Inc. are 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.58 (Maintenance), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.