Lornamead
FDA inspection history in Tonawanda, New York, 2023 to 2026
- 2
- Form 483s
Every document, by year
- Form 483
2023: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Tonawanda, New York.
- 2023The longest 483 on file: 5 observations over 5 pages at Tonawanda, New York.
- 2026One Form 483, at Tonawanda, New York.
Cited most
Across all Lornamead observations on file
- 21 CFR 211.198(a)Complaint files2
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.180(e)(2)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Lornamead file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
Tonawanda, New York
Two Form 483s · 2023 to 2026 · 8 observations
Latest: Form 483, Jan 21, 2026 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-21 | 483 Form 483 | Tonawanda, New York | 3 | $99 |
| 2023-04-11 | 483 Form 483 | Tonawanda, New York | 5 | $99 |
Investigators on these documents
FEI number 1000120219 · most recent document Jan 21, 2026
About Lornamead
How many FDA Form 483s has Lornamead received?
FDA Intel has 2 Form 483s on file for Lornamead; the most recent is dated Jan 21, 2026.
When was Lornamead last inspected by FDA?
The most recent FDA inspection document on file for Lornamead is a Form 483 dated Jan 21, 2026, for the site in Tonawanda, New York.
What did FDA cite at Lornamead?
The regulations cited most in the observations on file for Lornamead are 21 CFR 211.198(a) (Complaint files), 2 times; 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.180(e)(2) (General requirements), 1 time.