Meribel Pharma Strangnas AB
FDA inspection history in Strangnas, Sweden, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Strangnas, Sweden.
Cited most
Across all Meribel Pharma Strangnas AB observations on file
- 21 CFR 211.160General requirements2
- 21 CFR 211.25Personnel qualifications2
- 21 CFR 211.68Automatic, mechanical, and electronic equipment2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.142Warehousing procedures1
The complete Meribel Pharma Strangnas AB file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Strangnas, Sweden
One Form 483 · 2019 · 10 observations
Latest: Form 483, Sep 6, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-06 | 483 Form 483 | Strangnas, Sweden | 10 | $99 |
Investigators on these documents
FEI number 3006524831 · most recent document Sep 6, 2019
About Meribel Pharma Strangnas AB
How many FDA Form 483s has Meribel Pharma Strangnas AB received?
FDA Intel has 1 Form 483 on file for Meribel Pharma Strangnas AB; the most recent is dated Sep 6, 2019.
When was Meribel Pharma Strangnas AB last inspected by FDA?
The most recent FDA inspection document on file for Meribel Pharma Strangnas AB is a Form 483 dated Sep 6, 2019, for the site in Strangnas, Sweden.
What did FDA cite at Meribel Pharma Strangnas AB?
The regulations cited most in the observations on file for Meribel Pharma Strangnas AB are 21 CFR 211.160 (General requirements), 2 times; 21 CFR 211.25 (Personnel qualifications), 2 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 2 times.