Labcorp Early Development Laboratories
FDA inspection history in Greenfield, Indiana, 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 Greenfield, Indiana.
Cited most
Across all Labcorp Early Development Laboratories observations on file
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.166(a)(4)Stability testing1
- 21 CFR 211.192Production record review1
- 21 CFR 211.68(b)Automatic, mechanical, and electronic equipment1
The complete Labcorp Early Development Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Greenfield, Indiana
One Form 483 · 2025 · 4 observations
Latest: Form 483, Jul 25, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-07-25 | 483 Form 483 | Greenfield, Indiana | 4 | $99 |
Investigators on these documents
FEI number 1850039 · most recent document Jul 25, 2025
About Labcorp Early Development Laboratories
How many FDA Form 483s has Labcorp Early Development Laboratories received?
FDA Intel has 1 Form 483 on file for Labcorp Early Development Laboratories; the most recent is dated Jul 25, 2025.
When was Labcorp Early Development Laboratories last inspected by FDA?
The most recent FDA inspection document on file for Labcorp Early Development Laboratories is a Form 483 dated Jul 25, 2025, for the site in Greenfield, Indiana.
What did FDA cite at Labcorp Early Development Laboratories?
The regulations cited most in the observations on file for Labcorp Early Development Laboratories are 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.166(a)(4) (Stability testing), 1 time; 21 CFR 211.192 (Production record review), 1 time.