BAL PHARMA LIMITED
FDA inspection history in BENGALURU, India, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at BENGALURU, India.
Cited most
Across all BAL PHARMA LIMITED observations on file
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.87Retesting of approved components, drug product containers, and closures1
The complete BAL PHARMA LIMITED file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
BENGALURU, India
One Form 483 · 2018 · 5 observations
Latest: Form 483, Nov 16, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-11-16 | 483 Form 483 | BENGALURU, India | 5 | $99 |
FEI number 3006807057 · most recent document Nov 16, 2018
About BAL PHARMA LIMITED
How many FDA Form 483s has BAL PHARMA LIMITED received?
FDA Intel has 1 Form 483 on file for BAL PHARMA LIMITED; the most recent is dated Nov 16, 2018.
When was BAL PHARMA LIMITED last inspected by FDA?
The most recent FDA inspection document on file for BAL PHARMA LIMITED is a Form 483 dated Nov 16, 2018, for the site in BENGALURU, India.
What did FDA cite at BAL PHARMA LIMITED?
The regulations cited most in the observations on file for BAL PHARMA LIMITED are 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.87 (Retesting of approved components, drug product containers, and closures), 1 time.