# Milupa GmbH, Fulda, Germany – FDA Inspections

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

> Inspection records and compliance data for Milupa GmbH in Fulda. 14 FDA inspections on record, 2 Form 483s, last inspected May 09, 2025.

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## Details

- Name: Milupa GmbH
- FEI Number: 3004322174
- Address Line 1: Schleyerstr. 4
- City: Fulda
- Country Name: Germany
- Address: Schleyerstr. 4, Fulda, Germany
- Country: Germany

## Related Documents

- FDA Inspection 1270257 - Milupa GmbH - 2025-05-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2025
- [FDA Inspection 1270257 - Milupa GmbH - 2025-05-09](https://www.keypedia.com/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 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2025
- [EIR - Milupa GmbH - 2024-06-07](https://www.keypedia.com/records/eir/milupa-gmbh/f4444201-9efc-4ca7-8f66-21cbc4c9b0d8) — source: FDA, date: June 7, 2024
- [483 - Milupa GmbH - 2024-06-07](https://www.keypedia.com/records/483/milupa-gmbh/d402d244-a68c-4b2b-a599-34e8216d772e) — source: FDA, date: June 7, 2024
- FDA Inspection 1240572 - Milupa GmbH - 2024-06-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 7, 2024
- [FDA Inspection 1240572 - Milupa GmbH - 2024-06-07](https://www.keypedia.com/records/fda_inspections/milupa-gmbh/e54b8cd8-68ee-48b3-8378-b96eac54c515) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2024
- [EIR - Milupa GmbH - 2023-05-26](https://www.keypedia.com/records/eir/milupa-gmbh/63990ead-7d98-40b9-8a50-6fb14886fb11) — source: FDA, date: May 26, 2023
- [483 - Milupa GmbH - 2023-05-26](https://www.keypedia.com/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.keypedia.com/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 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- [EIR - Milupa GmbH - 2022-05-07](https://www.keypedia.com/records/eir/milupa-gmbh/5211a449-6c88-462a-9519-01135985b127) — source: FDA, date: May 7, 2022
- [483 - Milupa GmbH - 2022-05-07](https://www.keypedia.com/records/483/milupa-gmbh/0c715c20-e237-4378-be5d-65b03f586e75) — source: FDA, date: May 7, 2022
- FDA Inspection 1169133 - Milupa GmbH - 2022-05-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 7, 2022
- [FDA Inspection 1169133 - Milupa GmbH - 2022-05-07](https://www.keypedia.com/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 — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2019

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