Sidmak Laboratories (India) Pvt.Ltd.
FDA inspection history in Dehradun, India, 2023
- 1
- Form 483
Every document, by year
- Form 483
2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2023One Form 483, at Dehradun, India.
Cited most
Across all Sidmak Laboratories (India) Pvt.Ltd. observations on file
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.165Testing and release for distribution1
The complete Sidmak Laboratories (India) Pvt.Ltd. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Dehradun, India
One Form 483 · 2023 · 3 observations
Latest: Form 483, May 13, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-05-13 | 483 Form 483 | Dehradun, India | 3 | $99 |
Investigators on these documents
FEI number 3008127341 · most recent document May 13, 2023
About Sidmak Laboratories (India) Pvt.Ltd.
How many FDA Form 483s has Sidmak Laboratories (India) Pvt.Ltd. received?
FDA Intel has 1 Form 483 on file for Sidmak Laboratories (India) Pvt.Ltd.; the most recent is dated May 13, 2023.
When was Sidmak Laboratories (India) Pvt.Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Sidmak Laboratories (India) Pvt.Ltd. is a Form 483 dated May 13, 2023, for the site in Dehradun, India.
What did FDA cite at Sidmak Laboratories (India) Pvt.Ltd.?
The regulations cited most in the observations on file for Sidmak Laboratories (India) Pvt.Ltd. are 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times; 21 CFR 211.165 (Testing and release for distribution), 1 time.