# Nestle Nederland BV, Nunspeet, Netherlands – FDA Inspections

Source: https://www.keypedia.com/companies/nestle-nederland-bv/e9a73200-23b1-4de3-860a-3e5c24441126

> Inspection records and compliance data for Nestle Nederland BV in Nunspeet. 9 FDA inspections on record, 2 Form 483s, last inspected September 12, 2025.

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## Details

- Name: Nestle Nederland BV
- FEI Number: 3010969207
- Address Line 1: Laan 110
- City: Nunspeet
- Country Name: Netherlands
- Address: Laan 110, Nunspeet, Netherlands
- Country: Netherlands

## Related Documents

- FDA Inspection 1281244 - Nestle Nederland BV - 2025-09-12 — source: FDA, date: September 12, 2025
- [FDA Inspection 1281244 - Nestle Nederland BV - 2025-09-12](https://www.keypedia.com/records/fda_inspections/nestle-nederland-bv/df890e1c-ce19-4e27-bd42-10c72f20ce9c) — source: FDA, date: September 12, 2025
- FDA Inspection 1231417 - Nestle Nederland BV - 2024-09-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2024
- [FDA Inspection 1231417 - Nestle Nederland BV - 2024-09-06](https://www.keypedia.com/records/fda_inspections/nestle-nederland-bv/16b8938c-052b-4800-8cb3-a5000acc8b47) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2024
- FDA Inspection 1231417 - Nestle Nederland BV - 2024-09-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 6, 2024
- FDA Inspection 1221408 - Nestle Nederland BV - 2023-09-08 — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2023
- FDA Inspection 1221408 - Nestle Nederland BV - 2023-09-08 — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2023
- FDA Inspection 1180745 - Nestle Nederland BV - 2022-09-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2022
- FDA Inspection 1180745 - Nestle Nederland BV - 2022-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2022
- FDA Inspection 1097632 - Nestle Nederland BV - 2019-07-04 — classification: No Action Indicated (NAI), source: FDA, date: July 4, 2019

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