Satyadeeptha Pharmaceuticals Limited
FDA inspection history in Humnabad, 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 Humnabad, India.
Cited most
Across all Satyadeeptha Pharmaceuticals Limited observations on file
- 21 CFR 211.188Batch production and control records2
- 21 CFR 211.67Equipment cleaning and maintenance2
- 21 CFR 111
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
The complete Satyadeeptha Pharmaceuticals Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Humnabad, India
One Form 483 · 2018 · 13 observations
Latest: Form 483, Jan 11, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-01-11 | 483 Form 483 | Humnabad, India | 13 | $99 |
Investigators on these documents
FEI number 3013987923 · most recent document Jan 11, 2018
About Satyadeeptha Pharmaceuticals Limited
How many FDA Form 483s has Satyadeeptha Pharmaceuticals Limited received?
FDA Intel has 1 Form 483 on file for Satyadeeptha Pharmaceuticals Limited; the most recent is dated Jan 11, 2018.
When was Satyadeeptha Pharmaceuticals Limited last inspected by FDA?
The most recent FDA inspection document on file for Satyadeeptha Pharmaceuticals Limited is a Form 483 dated Jan 11, 2018, for the site in Humnabad, India.
What did FDA cite at Satyadeeptha Pharmaceuticals Limited?
The regulations cited most in the observations on file for Satyadeeptha Pharmaceuticals Limited are 21 CFR 211.188 (Batch production and control records), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 11, 1 time.