Qualified source record
NOTE Herrljunga AB
NOTE Herrljunga AB is listed in FDA device registration data in Herrljunga Vastra Gotaland, SE with the establishment role “Manufacture Medical Device for Another Party (Contract Manufacturer).” This qualified source record does not establish FDA approval, current capacity, or suitability for a project.
- Company type
- FDA-registered contract manufacturing establishment
- Source-reported role
- Manufacture Medical Device for Another Party (Contract Manufacturer)
- Source identifier
- 3018240701
- Owner/operator in source
- NOTE Herrljunga AB
- Company locations
- Herrljunga Vastra Gotaland, Sweden
Locality and country come from the registered establishment record; the registered street address is not republished.
- Services & equipment
- Industries served
- Source checked
- 2026-09-07
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