Knoll LLC
FDA inspection history in Jayuya, Puerto Rico, 2020 to 2024
- 2
- Form 483s
Every document, by year
- Form 483
2020: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Jayuya, Puerto Rico.
- 2020The longest 483 on file: 4 observations over 5 pages at Jayuya, Puerto Rico.
- 2024One Form 483, at Jayuya, Puerto Rico.
Cited most
Across all Knoll observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160(b)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
The complete Knoll 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
Jayuya, Puerto Rico
Two Form 483s · 2020 to 2024 · 6 observations
Latest: Form 483, Apr 18, 2024 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-18 | 483 Form 483 | Jayuya, Puerto Rico | 2 | $99 |
| 2020-02-20 | 483 Form 483 | Jayuya, Puerto Rico | 4 | $99 |
Investigators on these documents
FEI number 3000210838 · most recent document Apr 18, 2024
About Knoll LLC
How many FDA Form 483s has Knoll LLC received?
FDA Intel has 2 Form 483s on file for Knoll LLC; the most recent is dated Apr 18, 2024.
When was Knoll LLC last inspected by FDA?
The most recent FDA inspection document on file for Knoll LLC is a Form 483 dated Apr 18, 2024, for the site in Jayuya, Puerto Rico.
What did FDA cite at Knoll LLC?
The regulations cited most in the observations on file for Knoll LLC are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160(b) (General requirements), 1 time.