AIZANT DRUG RESEARCH SOLUTIONS PVT LTD
FDA inspection history in Hyderabad, India, 2020
- 1
- Form 483
Every document, by year
- Form 483
2020: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2020One Form 483, at Hyderabad, India.
Cited most
Across all AIZANT DRUG RESEARCH SOLUTIONS PVT observations on file
- 21 CFR 211.170Reserve samples1
- 21 CFR 211.186Master production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.52Washing and toilet facilities1
- 21 CFR 211.63Equipment design, size, and location1
The complete AIZANT DRUG RESEARCH SOLUTIONS PVT file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Hyderabad, India
One Form 483 · 2020 · 7 observations
Latest: Form 483, Jan 24, 2020 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2020-01-24 | 483 Form 483 | Hyderabad, India | 7 | $99 |
Investigators on these documents
FEI number 3008243902 · most recent document Jan 24, 2020
About AIZANT DRUG RESEARCH SOLUTIONS PVT LTD
How many FDA Form 483s has AIZANT DRUG RESEARCH SOLUTIONS PVT LTD received?
FDA Intel has 1 Form 483 on file for AIZANT DRUG RESEARCH SOLUTIONS PVT LTD; the most recent is dated Jan 24, 2020.
When was AIZANT DRUG RESEARCH SOLUTIONS PVT LTD last inspected by FDA?
The most recent FDA inspection document on file for AIZANT DRUG RESEARCH SOLUTIONS PVT LTD is a Form 483 dated Jan 24, 2020, for the site in Hyderabad, India.
What did FDA cite at AIZANT DRUG RESEARCH SOLUTIONS PVT LTD?
The regulations cited most in the observations on file for AIZANT DRUG RESEARCH SOLUTIONS PVT LTD are 21 CFR 211.170 (Reserve samples), 1 time; 21 CFR 211.186 (Master production and control records), 1 time; 21 CFR 211.192 (Production record review), 1 time.