Novo Nordisk Pharmaceutical Industries LP
FDA inspection history in Clayton, North Carolina, 2022 to 2023
- 2
- Form 483s
Every document, by year
- Form 483
2022: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022–23Two Form 483s, at Clayton, North Carolina.
- 2022The longest 483 on file: 3 observations over 4 pages at Clayton, North Carolina.
Cited most
Across all Novo Nordisk Pharmaceutical Industries observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.192Production record review1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Novo Nordisk Pharmaceutical Industries file.
All 2 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
Clayton, North Carolina
Two Form 483s · 2022 to 2023 · 5 observations
Latest: Form 483, Jul 13, 2023 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-07-13 | 483 Form 483 | Clayton, North Carolina | 2 | $99 |
| 2022-05-13 | 483 Form 483 | Clayton, North Carolina | 3 | $99 |
Investigators on these documents
FEI number 1000158576 · most recent document Jul 13, 2023
About Novo Nordisk Pharmaceutical Industries LP
How many FDA Form 483s has Novo Nordisk Pharmaceutical Industries LP received?
FDA Intel has 2 Form 483s on file for Novo Nordisk Pharmaceutical Industries LP; the most recent is dated Jul 13, 2023.
When was Novo Nordisk Pharmaceutical Industries LP last inspected by FDA?
The most recent FDA inspection document on file for Novo Nordisk Pharmaceutical Industries LP is a Form 483 dated Jul 13, 2023, for the site in Clayton, North Carolina.
What did FDA cite at Novo Nordisk Pharmaceutical Industries LP?
The regulations cited most in the observations on file for Novo Nordisk Pharmaceutical Industries LP are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.192 (Production record review), 1 time; 21 CFR 211.67 (Equipment cleaning and maintenance), 1 time.