Lonza Houston, Inc.
FDA inspection history in Houston, Texas, 2020
- 2
- Form 483s
Every document, by year
- Form 483
2020: two Form 483s.
The story so far
Built from the dates and citations on the documents themselves.
- 2020Two Form 483s, at Houston, Texas.
- 2020The longest 483 on file: 4 observations over 8 pages at Houston, Texas.
Cited most
Across all Lonza Houston observations on file
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.42Design and construction features2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
The complete Lonza Houston file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Houston, Texas
Two Form 483s · 2020 · 8 observations
Latest: Form 483, Dec 10, 2020 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-12-10 | 483 Form 483 | Houston, Texas | 4 | $99 |
| 2020-12-10 | 483 Form 483 | Houston, Texas | 4 | $99 |
Investigators on these documents
FEI number 3013629214 · most recent document Dec 10, 2020
About Lonza Houston, Inc.
How many FDA Form 483s has Lonza Houston, Inc. received?
FDA Intel has 2 Form 483s on file for Lonza Houston, Inc.; the most recent is dated Dec 10, 2020.
When was Lonza Houston, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Lonza Houston, Inc. is a Form 483 dated Dec 10, 2020, for the site in Houston, Texas.
What did FDA cite at Lonza Houston, Inc.?
The regulations cited most in the observations on file for Lonza Houston, Inc. are 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.42 (Design and construction features), 2 times.