Celeste Industries Corporation
FDA inspection history in Easton, Maryland, 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 Easton, Maryland.
Cited most
Across all Celeste Industries observations on file
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.165(e)Testing and release for distribution1
- 21 CFR 211.180(e)(1)General requirements1
- 21 CFR 211.194(a)(8)Laboratory records1
- 21 CFR 211.25(a)Personnel qualifications1
The complete Celeste Industries file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Easton, Maryland
One Form 483 · 2025 · 7 observations
Latest: Form 483, Feb 28, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-28 | 483 Form 483 | Easton, Maryland | 7 | $99 |
Investigators on these documents
FEI number 3012532308 · most recent document Feb 28, 2025
About Celeste Industries Corporation
How many FDA Form 483s has Celeste Industries Corporation received?
FDA Intel has 1 Form 483 on file for Celeste Industries Corporation; the most recent is dated Feb 28, 2025.
When was Celeste Industries Corporation last inspected by FDA?
The most recent FDA inspection document on file for Celeste Industries Corporation is a Form 483 dated Feb 28, 2025, for the site in Easton, Maryland.
What did FDA cite at Celeste Industries Corporation?
The regulations cited most in the observations on file for Celeste Industries Corporation are 21 CFR 211.160(a) (General requirements), 1 time; 21 CFR 211.165(e) (Testing and release for distribution), 1 time; 21 CFR 211.180(e)(1) (General requirements), 1 time.