MARKSANS PHARMA LIMITED
FDA inspection history in Verna, India, 2019 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Verna, India.
- 2019The longest 483 on file: 8 observations over 5 pages at Verna, India.
- 2023One Form 483, at Verna, India.
Cited most
Across all MARKSANS PHARMA LIMITED observations on file
- 21 CFR 211.166Stability testing2
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.160General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(a)Responsibilities of quality control unit1
The complete MARKSANS PHARMA LIMITED 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
Verna, India
Two Form 483s · 2019 to 2023 · 10 observations
Latest: Form 483, Aug 4, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-08-04 | 483 Form 483 | Verna, India | 2 | $99 |
| 2019-03-05 | 483 Form 483 | Verna, India | 8 | $99 |
FEI number 3006230648 · most recent document Aug 4, 2023
About MARKSANS PHARMA LIMITED
How many FDA Form 483s has MARKSANS PHARMA LIMITED received?
FDA Intel has 2 Form 483s on file for MARKSANS PHARMA LIMITED; the most recent is dated Aug 4, 2023.
When was MARKSANS PHARMA LIMITED last inspected by FDA?
The most recent FDA inspection document on file for MARKSANS PHARMA LIMITED is a Form 483 dated Aug 4, 2023, for the site in Verna, India.
What did FDA cite at MARKSANS PHARMA LIMITED?
The regulations cited most in the observations on file for MARKSANS PHARMA LIMITED are 21 CFR 211.166 (Stability testing), 2 times; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.160 (General requirements), 1 time.