Telix IsoTherapeutics Group, Inc.
FDA inspection history in Angleton, Texas, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Angleton, Texas.
Cited most
Across all Telix IsoTherapeutics Group observations on file
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.198Complaint files1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.42Design and construction features1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Telix IsoTherapeutics Group file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Angleton, Texas
One Form 483 · 2019 · 5 observations
Latest: Form 483, May 17, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-17 | 483 Form 483 | Angleton, Texas | 5 | $99 |
Investigators on these documents
FEI number 3007294884 · most recent document May 17, 2019
About Telix IsoTherapeutics Group, Inc.
How many FDA Form 483s has Telix IsoTherapeutics Group, Inc. received?
FDA Intel has 1 Form 483 on file for Telix IsoTherapeutics Group, Inc.; the most recent is dated May 17, 2019.
When was Telix IsoTherapeutics Group, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Telix IsoTherapeutics Group, Inc. is a Form 483 dated May 17, 2019, for the site in Angleton, Texas.
What did FDA cite at Telix IsoTherapeutics Group, Inc.?
The regulations cited most in the observations on file for Telix IsoTherapeutics Group, Inc. are 21 CFR 211.130 (Packaging and labeling operations), 1 time; 21 CFR 211.198 (Complaint files), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.