Ceela Naturals
FDA inspection history in Louisville, Kentucky, 2021
- 1
- Form 483
Every document, by year
- Form 483
2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2021One Form 483, at Louisville, Kentucky.
Cited most
Across all Ceela Naturals observations on file
- 21 CFR 211.100(a)Written procedures; deviations2
- 21 CFR 211.125(a)Labeling issuance1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.84(d)(1)Testing and approval or rejection of components, drug product containers, and closures1
The complete Ceela Naturals file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Louisville, Kentucky
One Form 483 · 2021 · 5 observations
Latest: Form 483, Aug 31, 2021 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-08-31 | 483 Form 483 | Louisville, Kentucky | 5 | $99 |
Investigators on these documents
FEI number 3009528637 · most recent document Aug 31, 2021
About Ceela Naturals
How many FDA Form 483s has Ceela Naturals received?
FDA Intel has 1 Form 483 on file for Ceela Naturals; the most recent is dated Aug 31, 2021.
When was Ceela Naturals last inspected by FDA?
The most recent FDA inspection document on file for Ceela Naturals is a Form 483 dated Aug 31, 2021, for the site in Louisville, Kentucky.
What did FDA cite at Ceela Naturals?
The regulations cited most in the observations on file for Ceela Naturals are 21 CFR 211.100(a) (Written procedures; deviations), 2 times; 21 CFR 211.125(a) (Labeling issuance), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.