# Neochild, LLC - Inspection Records

Source: https://www.keypedia.com/companies/neochild-llc/659ba1af-668f-44a0-8581-045a73af9130

> Inspection records and compliance data for Neochild, LLC in Oklahoma City, Oklahoma. Access full analysis and detailed observations.

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## Details

- Name: Neochild, LLC
- FEI Number: 3006271008
- City: Oklahoma City
- State: Oklahoma
- Country Name: United States
- Address Line 1: 8213 Sw 23rd Pl
- Zip Code: 73128

## Related Documents

- [FDA Inspection 1305038 - Neochild, LLC - 2026-02-11](https://www.keypedia.com/records/fda_inspections/neochild-llc/707ec9b8-b414-4600-abc9-c5cd536aa40c) — source: FDA, date: February 11, 2026
- [FDA Inspection 1305038 - Neochild, LLC - 2026-02-11](https://www.keypedia.com/records/fda_inspections/neochild-llc/3d524811-a3b5-4798-833d-bc9d58ecf4d0) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2026
- [FDA Inspection 1305038 - Neochild, LLC - 2026-02-11](https://www.keypedia.com/records/fda_inspections/neochild-llc/99ed40cb-e2d8-474a-8e09-5464d9c2729c) — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2026
- [FDA Inspection 950996 - Neochild, LLC - 2015-10-30](https://www.keypedia.com/records/fda_inspections/neochild-llc/569b0738-c755-4d42-9608-3e9ffe658c89) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2015
- [FDA Inspection 950996 - Neochild, LLC - 2015-10-30](https://www.keypedia.com/records/fda_inspections/neochild-llc/cb08a370-9b4e-4ca5-a74d-a221750d9852) — classification: No Action Indicated (NAI), source: FDA, date: October 30, 2015
- [FDA Inspection 647598 - Neochild, LLC - 2010-02-04](https://www.keypedia.com/records/fda_inspections/neochild-llc/e4f934a2-84b9-41e9-ac08-17067b18e274) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 4, 2010
- [FDA Inspection 647598 - Neochild, LLC - 2010-02-04](https://www.keypedia.com/records/fda_inspections/neochild-llc/4e21655f-a6bc-4554-a2e9-2e479bc3a373) — classification: No Action Indicated (NAI), source: FDA, date: February 4, 2010

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