Smilax Laboratories Limited
FDA inspection history in Visakhapatnam, India, 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 Visakhapatnam, India.
Cited most
Across all Smilax Laboratories Limited observations on file
- 21 CFR 211.192Production record review1
- 21 CFR 211.198Complaint files1
The complete Smilax Laboratories Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Visakhapatnam, India
One Form 483 · 2023
Latest: Form 483, Sep 15, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-15 | 483 Form 483 | Visakhapatnam, India | — | $99 |
FEI number 3008772334 · most recent document Sep 15, 2023
About Smilax Laboratories Limited
How many FDA Form 483s has Smilax Laboratories Limited received?
FDA Intel has 1 Form 483 on file for Smilax Laboratories Limited; the most recent is dated Sep 15, 2023.
When was Smilax Laboratories Limited last inspected by FDA?
The most recent FDA inspection document on file for Smilax Laboratories Limited is a Form 483 dated Sep 15, 2023, for the site in Visakhapatnam, India.
What did FDA cite at Smilax Laboratories Limited?
The regulations cited most in the observations on file for Smilax Laboratories Limited are 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.198 (Complaint files), 1 time.