LFB USA, Inc.
FDA inspection history in Charlton, Massachusetts, 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 Charlton, Massachusetts.
Cited most
Across all LFB USA observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.160General requirements2
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.180General requirements1
- 21 CFR 211.188Batch production and control records1
The complete LFB USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Charlton, Massachusetts
One Form 483 · 2022
Latest: Form 483, Apr 8, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-04-08 | 483 Form 483 | Charlton, Massachusetts | — | $99 |
Investigators on these documents
FEI number 3013501870 · most recent document Apr 8, 2022
About LFB USA, Inc.
How many FDA Form 483s has LFB USA, Inc. received?
FDA Intel has 1 Form 483 on file for LFB USA, Inc.; the most recent is dated Apr 8, 2022.
When was LFB USA, Inc. last inspected by FDA?
The most recent FDA inspection document on file for LFB USA, Inc. is a Form 483 dated Apr 8, 2022, for the site in Charlton, Massachusetts.
What did FDA cite at LFB USA, Inc.?
The regulations cited most in the observations on file for LFB USA, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.194 (Laboratory records), 2 times.