# H V Manufacturing - Inspection Records

Source: https://www.globalkeysolutions.net/companies/h-v-manufacturing/ef8aa493-1299-4441-b216-73f5cc702ab1

> Inspection records and compliance data for H V Manufacturing in Wheeling, Illinois. Access full analysis and detailed observations.

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## Details

- Name: H V Manufacturing
- FEI Number: 1480113
- City: Wheeling
- State: Illinois
- Country Name: United States
- Address Line 1: 1197 Willis Ave
- Zip Code: 60090

## Related Documents

- [FDA Inspection 1283290 - H V Manufacturing - 2026-03-13](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/a517ba6d-c7c8-4212-8055-f5962ceba0c3) — source: FDA, date: March 13, 2026
- [FDA Inspection 1283290 - H V Manufacturing - 2026-03-13](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/d6677798-802f-45b4-b9b2-6a7936c251f4) — source: FDA, date: March 13, 2026
- [FDA Inspection 1283288 - H V Manufacturing - 2026-03-13](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/e76aaddc-7b3c-486e-b5aa-8c1fe2c93ab4) — source: FDA, date: March 13, 2026
- [FDA Inspection 1115357 - H V Manufacturing - 2020-01-09](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/de8cfa93-dee4-461d-9586-fb503a0bb10d) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2020
- [FDA Inspection 1115357 - H V Manufacturing - 2020-01-09](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/d2f70d2d-b3fa-45b9-881b-b9049434aad7) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2020
- [FDA Inspection 1005171 - H V Manufacturing - 2016-12-28](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/bae7dd76-0537-4f13-bded-e88ac6126ac4) — classification: No Action Indicated (NAI), source: FDA, date: December 28, 2016
- [FDA Inspection 882389 - H V Manufacturing - 2014-04-30](https://www.globalkeysolutions.net/records/fda_inspections/h-v-manufacturing/8f6a192f-816d-471d-aec3-b6bcba24c590) — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2014

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