Apotek Production & Laboratorier AB
FDA inspection history in Umea, Sweden, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at Umea, Sweden.
Cited most
Across all Apotek Production & Laboratorier AB observations on file
- 21 CFR 211.113Control of microbiological contamination2
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.160General requirements1
- 21 CFR 211.167Special testing requirements1
- 21 CFR 211.188Batch production and control records1
The complete Apotek Production & Laboratorier AB file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Umea, Sweden
One Form 483 · 2026 · 9 observations
Latest: Form 483, Jan 29, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-29 | 483 Form 483 | Umea, Sweden | 9 | $99 |
Investigators on these documents
FEI number 3003766921 · most recent document Jan 29, 2026
About Apotek Production & Laboratorier AB
How many FDA Form 483s has Apotek Production & Laboratorier AB received?
FDA Intel has 1 Form 483 on file for Apotek Production & Laboratorier AB; the most recent is dated Jan 29, 2026.
When was Apotek Production & Laboratorier AB last inspected by FDA?
The most recent FDA inspection document on file for Apotek Production & Laboratorier AB is a Form 483 dated Jan 29, 2026, for the site in Umea, Sweden.
What did FDA cite at Apotek Production & Laboratorier AB?
The regulations cited most in the observations on file for Apotek Production & Laboratorier AB are 21 CFR 211.113 (Control of microbiological contamination), 2 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.160 (General requirements), 1 time.