# BASF AS avd Sandefjord - Inspection Records

Source: https://www.keypedia.com/companies/basf-as-avd-sandefjord/1b76cb86-c9db-45f9-bfdd-e2eaec2a67b7

> Inspection records and compliance data for BASF AS avd Sandefjord in Sandefjord, None. Access full analysis and detailed observations.

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## Details

- Name: BASF AS avd Sandefjord
- FEI Number: 3000212124
- City: Sandefjord
- State: None
- Country Name: Norway
- Address Line 1: Framnesveien 41
- Zip Code: None
- Business Operations: API MANUFACTURE

## Related Documents

- [483 - BASF AS avd Sandefjord - 2025-01-24](https://www.keypedia.com/records/483/basf-as-avd-sandefjord/9555c292-ac78-4a38-b8b0-3b3847d66e1d) — source: FDA, date: January 24, 2025
- [483 - BASF AS avd Sandefjord - 2025-01-24](https://www.keypedia.com/records/483/basf-as-avd-sandefjord/97b80de6-91fe-45d7-bccf-6b4740079fe9) — source: FDA, date: January 24, 2025
- [FDA Inspection 1260691 - BASF AS avd Sandefjord - 2025-01-24](https://www.keypedia.com/records/fda_inspections/basf-as-avd-sandefjord/f29d8e4f-3179-4222-a754-0ffffd25775e) — source: FDA, date: January 24, 2025
- [FDA Inspection 1260691 - BASF AS avd Sandefjord - 2025-01-24](https://www.keypedia.com/records/fda_inspections/basf-as-avd-sandefjord/ae30e5ba-8e08-4eee-baaf-5c9699e3e6a6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2025
- [FDA Inspection 1103527 - BASF AS avd Sandefjord - 2019-08-23](https://www.keypedia.com/records/fda_inspections/basf-as-avd-sandefjord/9442c62f-c86d-47b3-94ea-af5eeaf978ab) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2019
- [FDA Inspection 959713 - BASF AS avd Sandefjord - 2015-12-11](https://www.keypedia.com/records/fda_inspections/basf-as-avd-sandefjord/ab7a5801-7bfc-4917-9ccb-78c25a9094e0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 11, 2015
- [FDA Inspection 779878 - BASF AS avd Sandefjord - 2012-03-15](https://www.keypedia.com/records/fda_inspections/basf-as-avd-sandefjord/8ed6d957-c0e0-4999-9abf-733b258bcc34) — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2012

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