Ecolab Inc.
FDA inspection history in Huntington, Indiana, 2016 to 2025
- 3
- Form 483s
Every document, by year
- Form 483
2016: one Form 483; 2018: one Form 483; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2016–18Two Form 483s, at Huntington, Indiana.
- 2025One Form 483, at Huntington, Indiana.
- 2025The longest 483 on file: 5 observations over 5 pages at Huntington, Indiana.
Cited most
Across all Ecolab observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.22Responsibilities of quality control unit2
- 21 CFR 211.84Testing and approval or rejection of components, drug product containers, and closures2
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113(a)Control of microbiological contamination1
The complete Ecolab file.
All 3 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
Huntington, Indiana
Three Form 483s · 2016 to 2025 · 12 observations
Latest: Form 483, Jun 5, 2025 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-06-05 | 483 Form 483 | Huntington, Indiana | 5 | $99 |
| 2018-11-09 | 483 Form 483 | Huntington, Indiana | 3 | $99 |
| 2016-06-24 | 483 Form 483 | Huntington, Indiana | 4 | $99 |
Investigators on these documents
Andrew O. Ejiofor (1)Emilie Kahn (1)Robert M. Barbosa (1)Sarah E. Rhoades (1)
FEI number 1810414 · most recent document Jun 5, 2025
About Ecolab Inc.
How many FDA Form 483s has Ecolab Inc. received?
FDA Intel has 3 Form 483s on file for Ecolab Inc.; the most recent is dated Jun 5, 2025.
When was Ecolab Inc. last inspected by FDA?
The most recent FDA inspection document on file for Ecolab Inc. is a Form 483 dated Jun 5, 2025, for the site in Huntington, Indiana.
What did FDA cite at Ecolab Inc.?
The regulations cited most in the observations on file for Ecolab Inc. are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.22 (Responsibilities of quality control unit), 2 times; 21 CFR 211.84 (Testing and approval or rejection of components, drug product containers, and closures), 2 times.