# Milupa GmbH - Inspection Records

Source: https://www.globalkeysolutions.net/companies/milupa-gmbh/a406d6b0-df46-4822-8cfb-732831ba1f7c

> Inspection records and compliance data for Milupa GmbH in Fulda, None. Access full analysis and detailed observations.

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## Details

- Name: Milupa GmbH
- FEI Number: 3004322174
- City: Fulda
- State: None
- Country Name: Germany
- Address Line 1: Schleyerstr. 4
- Zip Code: None

## Related Documents

- [FDA Inspection 1270257 - Milupa GmbH - 2025-05-09](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/dad8f5bf-3591-4e9e-85ab-d7302b276e9b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2025
- [FDA Inspection 1270257 - Milupa GmbH - 2025-05-09](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/5d35f624-e0f6-4437-91da-90af5e742fdc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2025
- [FDA Inspection 1270257 - Milupa GmbH - 2025-05-09](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/f60c1600-da4a-4efd-bb53-bd44a5332539) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2025
- [483 - Milupa GmbH - 2024-06-07](https://www.globalkeysolutions.net/records/483/milupa-gmbh/d402d244-a68c-4b2b-a599-34e8216d772e) — source: FDA, date: June 7, 2024
- [FDA Inspection 1240572 - Milupa GmbH - 2024-06-07](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/e54b8cd8-68ee-48b3-8378-b96eac54c515) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2024
- [FDA Inspection 1240572 - Milupa GmbH - 2024-06-07](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/013c556f-0430-48af-b0cb-cd9960e766b1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2024
- [483 - Milupa GmbH - 2023-05-26](https://www.globalkeysolutions.net/records/483/milupa-gmbh/ae62f52e-4dcc-4d4a-b2d7-ca996dda474b) — source: FDA, date: May 26, 2023
- [FDA Inspection 1206439 - Milupa GmbH - 2023-05-26](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/dd5c81b4-0e79-4e61-b563-f808653cbd33) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- [FDA Inspection 1206439 - Milupa GmbH - 2023-05-26](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/cace5c94-4930-4f31-bdba-5bdf0c28d2a9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- [483 - Milupa GmbH - 2022-05-07](https://www.globalkeysolutions.net/records/483/milupa-gmbh/0c715c20-e237-4378-be5d-65b03f586e75) — source: FDA, date: May 7, 2022
- [FDA Inspection 1169133 - Milupa GmbH - 2022-05-07](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/3f2061c8-26fa-4ab0-8e4b-41ca46cdadec) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2022
- [FDA Inspection 1169133 - Milupa GmbH - 2022-05-07](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/5b0186e6-c896-489b-9f83-b73e53eb0c4b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2022
- [FDA Inspection 1109272 - Milupa GmbH - 2019-09-27](https://www.globalkeysolutions.net/records/fda_inspections/milupa-gmbh/14830b3d-9f99-41e3-bae5-315f0c6f91ba) — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2019

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