Intermed
FDA inspection history in Chennai, 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 Chennai, India.
Cited most
Across all Intermed observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122(d)Materials examination and usage criteria1
- 21 CFR 211.165(d)Testing and release for distribution1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete Intermed file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chennai, India
One Form 483 · 2023 · 6 observations
Latest: Form 483, Mar 17, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-03-17 | 483 Form 483 | Chennai, India | 6 | $99 |
Investigators on these documents
FEI number 3005202412 · most recent document Mar 17, 2023
About Intermed
How many FDA Form 483s has Intermed received?
FDA Intel has 1 Form 483 on file for Intermed; the most recent is dated Mar 17, 2023.
When was Intermed last inspected by FDA?
The most recent FDA inspection document on file for Intermed is a Form 483 dated Mar 17, 2023, for the site in Chennai, India.
What did FDA cite at Intermed?
The regulations cited most in the observations on file for Intermed are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.122(d) (Materials examination and usage criteria), 1 time; 21 CFR 211.165(d) (Testing and release for distribution), 1 time.