BASF Corporation
FDA inspection history in East Setauket, New York, 2017 to 2025
- 2
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at East Setauket, New York.
- 2025One Form 483, at East Setauket, New York.
- 2025The longest 483 on file: 4 observations over 18 pages at East Setauket, New York.
Cited most
Across all BASF observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.63Equipment design, size, and location1
- 21 CFR 58.190Storage and retrieval of records and data1
The complete BASF file.
All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
East Setauket, New York
Two Form 483s · 2017 to 2025 · 8 observations
Latest: Form 483, May 29, 2025 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-05-29 | 483 Form 483 | East Setauket, New York | 4 | $99 |
| 2017-11-17 | 483 Form 483 | East Setauket, New York | 4 | $99 |
Investigators on these documents
Chelsea W. Lamm (1)Corrine M. Carter (1)Mindy M. Chou (1)Orrine Arter (1)
FEI number 1000521506 · most recent document May 29, 2025
About BASF Corporation
How many FDA Form 483s has BASF Corporation received?
FDA Intel has 2 Form 483s on file for BASF Corporation; the most recent is dated May 29, 2025.
When was BASF Corporation last inspected by FDA?
The most recent FDA inspection document on file for BASF Corporation is a Form 483 dated May 29, 2025, for the site in East Setauket, New York.
What did FDA cite at BASF Corporation?
The regulations cited most in the observations on file for BASF Corporation are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.