Isorx Cyclotron Center
FDA inspection history in Lubbock, Texas, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Lubbock, Texas.
Cited most
Across all Isorx Cyclotron Center observations on file
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.113Control of microbiological contamination1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.192Production record review1
The complete Isorx Cyclotron Center file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lubbock, Texas
One Form 483 · 2026 · 7 observations
Latest: Form 483, Mar 13, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-13 | 483 Form 483 | Lubbock, Texas | 7 | $99 |
Investigators on these documents
FEI number 3021621451 · most recent document Mar 13, 2026
About Isorx Cyclotron Center
How many FDA Form 483s has Isorx Cyclotron Center received?
FDA Intel has 1 Form 483 on file for Isorx Cyclotron Center; the most recent is dated Mar 13, 2026.
When was Isorx Cyclotron Center last inspected by FDA?
The most recent FDA inspection document on file for Isorx Cyclotron Center is a Form 483 dated Mar 13, 2026, for the site in Lubbock, Texas.
What did FDA cite at Isorx Cyclotron Center?
The regulations cited most in the observations on file for Isorx Cyclotron Center are 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.188 (Batch production and control records), 2 times; 21 CFR 211.113 (Control of microbiological contamination), 1 time.