Nukemed, Inc dba SpectronRx
FDA inspection history in SOUTH BEND, Indiana, 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 SOUTH BEND, Indiana.
Cited most
Across all Nukemed, Inc dba SpectronRx observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.42Design and construction features1
The complete Nukemed, Inc dba SpectronRx file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
SOUTH BEND, Indiana
One Form 483 · 2022 · 2 observations
Latest: Form 483, May 12, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-05-12 | 483 Form 483 | SOUTH BEND, Indiana | 2 | $99 |
FEI number 3005176775 · most recent document May 12, 2022
About Nukemed, Inc dba SpectronRx
How many FDA Form 483s has Nukemed, Inc dba SpectronRx received?
FDA Intel has 1 Form 483 on file for Nukemed, Inc dba SpectronRx; the most recent is dated May 12, 2022.
When was Nukemed, Inc dba SpectronRx last inspected by FDA?
The most recent FDA inspection document on file for Nukemed, Inc dba SpectronRx is a Form 483 dated May 12, 2022, for the site in SOUTH BEND, Indiana.
What did FDA cite at Nukemed, Inc dba SpectronRx?
The regulations cited most in the observations on file for Nukemed, Inc dba SpectronRx are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.42 (Design and construction features), 1 time.