The Harvard Drug Group LLC dba Major
FDA inspection history in La Vergne, Tennessee, 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 La Vergne, Tennessee.
Cited most
Across all The Harvard Drug Group LLC dba Major observations on file
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete The Harvard Drug Group LLC dba Major file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
La Vergne, Tennessee
One Form 483 · 2026 · 1 observation
Latest: Form 483, Mar 20, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-20 | 483 Form 483 | La Vergne, Tennessee | 1 | $99 |
Investigators on these documents
FEI number 1818658 · most recent document Mar 20, 2026
About The Harvard Drug Group LLC dba Major
How many FDA Form 483s has The Harvard Drug Group LLC dba Major received?
FDA Intel has 1 Form 483 on file for The Harvard Drug Group LLC dba Major; the most recent is dated Mar 20, 2026.
When was The Harvard Drug Group LLC dba Major last inspected by FDA?
The most recent FDA inspection document on file for The Harvard Drug Group LLC dba Major is a Form 483 dated Mar 20, 2026, for the site in La Vergne, Tennessee.
What did FDA cite at The Harvard Drug Group LLC dba Major?
The regulations cited most in the observations on file for The Harvard Drug Group LLC dba Major are 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.