Maiva Pharma Private Limited
FDA inspection history in Hosur, India, 2019 to 2026
- 3
- Form 483s
Every document, by year
- Form 483
2019: one Form 483; 2022: one Form 483; 2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Hosur, India.
- 2022One Form 483, at Hosur, India.
- 2026One Form 483, at Hosur, India.
- 2026The longest 483 on file: 9 observations over 26 pages at Hosur, India.
Cited most
Across all Maiva Pharma Private Limited observations on file
- 21 CFR 211.113Control of microbiological contamination4
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.192Production record review2
- 21 CFR 211.42Design and construction features2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
The complete Maiva Pharma Private Limited file.
All 3 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
Hosur, India
Three Form 483s · 2019 to 2026 · 17 observations
Latest: Form 483, Feb 20, 2026 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-20 | 483 Form 483 | Hosur, India | 9 | $99 |
| 2022-10-29 | 483 Form 483 | Hosur, India | 6 | $99 |
| 2019-08-02 | 483 Form 483 | Hosur, India | 2 | $99 |
Investigators on these documents
Alan A. Rivera (1)Dipesh K. Shah (1)Jose E. Melendez (1)Samina S. Khan (1)Thomas J. Arista (1)
FEI number 3014362214 · most recent document Feb 20, 2026
About Maiva Pharma Private Limited
How many FDA Form 483s has Maiva Pharma Private Limited received?
FDA Intel has 3 Form 483s on file for Maiva Pharma Private Limited; the most recent is dated Feb 20, 2026.
When was Maiva Pharma Private Limited last inspected by FDA?
The most recent FDA inspection document on file for Maiva Pharma Private Limited is a Form 483 dated Feb 20, 2026, for the site in Hosur, India.
What did FDA cite at Maiva Pharma Private Limited?
The regulations cited most in the observations on file for Maiva Pharma Private Limited are 21 CFR 211.113 (Control of microbiological contamination), 4 times; 21 CFR 211.188 (Batch production and control records), 2 times; 21 CFR 211.192 (Production record review), 2 times.