Company
SwedenRechon Life Science AB, Limhamn, Sweden – FDA Inspections
Inspection records and compliance data for Rechon Life Science AB in Limhamn. 8 FDA inspections on record (1 OAI), 3 Form 483s, 1 warning letter, last inspected September 06, 2024.
Company Profile
This profile covers Rechon Life Science AB based in Limhamn, Sweden.
FDA Inspection History
- FDA inspections
- 8
- OAI
- 1
- VAI
- 5
- NAI
- 1
- Unclassified
- 1
- Form 483s
- 3
- Warning letters
- 1
First inspected September 16, 2011. Last inspected September 6, 2024.
FDA inspections (8)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| September 6, 2024 | OAI | Human Drugs · Drug Quality Assurance | 1251480 |
| March 17, 2023 | Not classified | Human Drugs | 1201600 |
| November 27, 2019 | VAI | Human Drugs · Drug Quality Assurance | 1125627 |
| June 29, 2018 | VAI | Human Drugs · Drug Quality Assurance | 1060687 |
| June 2, 2016 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 983550 |
| April 29, 2016 | VAI | Human Drugs · Drug Quality Assurance | 969057 |
| March 21, 2014 | VAI | Human Drugs · Drug Quality Assurance | 871626 |
| September 16, 2011 | VAI | Human Drugs · Drug Quality Assurance | 748168 |
FDA documents
Warning Letters (1)
People (6)
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Company Information
Name
Rechon Life Science AB
FEI Number
3002806978
Address
Soldattorpsvagen 5, Limhamn, Sweden
Country
Sweden
ID: ce84eed4-ada6-40a0-9005-2c2d6bbd729d