Partner Therapeutics, Inc.
FDA inspection history in Lynnwood, Washington, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Lynnwood, Washington.
Cited most
Across all Partner Therapeutics observations on file
- 21 CFR 211.166Stability testing1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Partner Therapeutics file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lynnwood, Washington
One Form 483 · 2022 · 3 observations
Latest: Form 483, Jul 22, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-07-22 | 483 Form 483 | Lynnwood, Washington | 3 | $99 |
FEI number 3007934434 · most recent document Jul 22, 2022
About Partner Therapeutics, Inc.
How many FDA Form 483s has Partner Therapeutics, Inc. received?
FDA Intel has 1 Form 483 on file for Partner Therapeutics, Inc.; the most recent is dated Jul 22, 2022.
When was Partner Therapeutics, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Partner Therapeutics, Inc. is a Form 483 dated Jul 22, 2022, for the site in Lynnwood, Washington.
What did FDA cite at Partner Therapeutics, Inc.?
The regulations cited most in the observations on file for Partner Therapeutics, Inc. are 21 CFR 211.166 (Stability testing), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.