Lilly del Caribe, Inc.
FDA inspection history in Carolina, Puerto Rico, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Carolina, Puerto Rico.
Cited most
Across all Lilly del Caribe observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete Lilly del Caribe file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Carolina, Puerto Rico
One Form 483 · 2023 · 2 observations
Latest: Form 483, Feb 17, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-02-17 | 483 Form 483 | Carolina, Puerto Rico | 2 | $99 |
Investigators on these documents
Angelica M. Hernandez (1)Jose Velez (1)Marian E. Ramirez (1)
FEI number 3004525072 · most recent document Feb 17, 2023
About Lilly del Caribe, Inc.
How many FDA Form 483s has Lilly del Caribe, Inc. received?
FDA Intel has 1 Form 483 on file for Lilly del Caribe, Inc.; the most recent is dated Feb 17, 2023.
When was Lilly del Caribe, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Lilly del Caribe, Inc. is a Form 483 dated Feb 17, 2023, for the site in Carolina, Puerto Rico.
What did FDA cite at Lilly del Caribe, Inc.?
The regulations cited most in the observations on file for Lilly del Caribe, Inc. are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time.