INPO AS
Medizin- & Gesundheitsbedarf, Norwegen
INPO AS ist ein Unternehmen im Bereich Medizin- & Gesundheitsbedarf mit Sitz in Årnes, Norwegen. Eingetragen in einem öffentlichen Unternehmensregister.
- Type
- brand seeking distribution
- Location
- Årnes, Norway
- Founded
- 2021
- Website
- https://inpo.no
- Categories
- Medizin- & Gesundheitsbedarf
Listed in a source registry
Verified facts
- debarment-clear (green), checked 2026-08-14 OpenSanctions
- sanctions-clear (green), checked 2026-08-14 OpenSanctions
- domain-registered (green), checked 2026-08-14 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-14 Mail server of the company domain
- registry-active-global (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- tax-filing-active (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- workforce-on-record (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- public-contract-awarded (green), checked 2026-02-03 TED (Tenders Electronic Daily), EU public procurement award notices Hier trägt der Zuschlag zusätzlich eine fremde Prüfung: In der EU und im EWR muss ein öffentlicher Auftraggeber Bieter ausschließen, die wegen Betrugs, Korruption oder Geldwäsche verurteilt sind, sowie solche, bei denen rechtskräftig festgestellte Steuer- oder Sozialabgabenschulden bestehen. Directive 2014/24/EU, Article 57 (exclusion grounds)
- registry-activity (green), checked 2026-08-23 Norway Brønnøysund Register Centre (open bulk file)
- leadership-on-record (green), checked 2026-08-14 Brønnøysund (roller)
- annual-accounts-filed (green), checked 2026-08-14 Regnskapsregisteret (Brønnøysund)
- registry-id-verified (green), checked 2026-07-11 Bronnoysund Register Centre, Central Coordinating Register of Legal Entities (Enhetsregisteret)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)