Loba Feinchemie GmbH
FDA inspection history in Fischamend, Austria, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Fischamend, Austria.
Cited most
Across all Loba Feinchemie observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.192Production record review2
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Loba Feinchemie file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Fischamend, Austria
One Form 483 · 2025 · 7 observations
Latest: Form 483, Nov 11, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-11-11 | 483 Form 483 | Fischamend, Austria | 7 | $99 |
Investigators on these documents
FEI number 3002807485 · most recent document Nov 11, 2025
About Loba Feinchemie GmbH
How many FDA Form 483s has Loba Feinchemie GmbH received?
FDA Intel has 1 Form 483 on file for Loba Feinchemie GmbH; the most recent is dated Nov 11, 2025.
When was Loba Feinchemie GmbH last inspected by FDA?
The most recent FDA inspection document on file for Loba Feinchemie GmbH is a Form 483 dated Nov 11, 2025, for the site in Fischamend, Austria.
What did FDA cite at Loba Feinchemie GmbH?
The regulations cited most in the observations on file for Loba Feinchemie GmbH are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.186 (Master production and control records), 1 time.