Packpharm Limited
FDA inspection history in Norwich, United Kingdom, 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 Norwich, United Kingdom.
Cited most
Across all Packpharm Limited observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.160General requirements1
- 21 CFR 211.58Maintenance1
The complete Packpharm Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Norwich, United Kingdom
One Form 483 · 2023 · 3 observations
Latest: Form 483, Sep 1, 2023 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-09-01 | 483 Form 483 | Norwich, United Kingdom | 3 | $99 |
FEI number 3027274110 · most recent document Sep 1, 2023
About Packpharm Limited
How many FDA Form 483s has Packpharm Limited received?
FDA Intel has 1 Form 483 on file for Packpharm Limited; the most recent is dated Sep 1, 2023.
When was Packpharm Limited last inspected by FDA?
The most recent FDA inspection document on file for Packpharm Limited is a Form 483 dated Sep 1, 2023, for the site in Norwich, United Kingdom.
What did FDA cite at Packpharm Limited?
The regulations cited most in the observations on file for Packpharm Limited are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.58 (Maintenance), 1 time.