Sun Pharmaceutical Industries, Inc
FDA inspection history in Cranbury, New Jersey, 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 Cranbury, New Jersey.
Cited most
Across all Sun Pharmaceutical Industries observations on file
- 21 CFR 211.192Production record review2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.130Packaging and labeling operations1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.58Maintenance1
The complete Sun Pharmaceutical Industries file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Cranbury, New Jersey
One Form 483 · 2018 · 8 observations
Latest: Form 483, Mar 9, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-03-09 | 483 Form 483 | Cranbury, New Jersey | 8 | $99 |
Investigators on these documents
FEI number 3005551493 · most recent document Mar 9, 2018
About Sun Pharmaceutical Industries, Inc
How many FDA Form 483s has Sun Pharmaceutical Industries, Inc received?
FDA Intel has 1 Form 483 on file for Sun Pharmaceutical Industries, Inc; the most recent is dated Mar 9, 2018.
When was Sun Pharmaceutical Industries, Inc last inspected by FDA?
The most recent FDA inspection document on file for Sun Pharmaceutical Industries, Inc is a Form 483 dated Mar 9, 2018, for the site in Cranbury, New Jersey.
What did FDA cite at Sun Pharmaceutical Industries, Inc?
The regulations cited most in the observations on file for Sun Pharmaceutical Industries, Inc are 21 CFR 211.192 (Production record review), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.130 (Packaging and labeling operations), 1 time.