# Interpac Technologies, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/interpac-technologies-inc/5e8078c2-97e4-4af1-b6f8-87654e945cf0

> Inspection records and compliance data for Interpac Technologies, Inc. in Woodland, California. Access full analysis and detailed observations.

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## Details

- Name: Interpac Technologies, Inc.
- FEI Number: 2935764
- City: Woodland
- State: California
- Country Name: United States
- Address Line 1: 260 N Pioneer Ave
- Zip Code: 95776

## Related Documents

- [FDA Inspection 1241500 - Interpac Technologies, Inc. - 2024-09-20](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/f5c6eef4-8b9c-4ecd-9016-6ec5b2419320) — source: FDA, date: September 20, 2024
- [FDA Inspection 1241500 - Interpac Technologies, Inc. - 2024-09-20](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/a7bf6b5b-7bdc-4ada-bbf1-26246c887628) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2024
- [FDA Inspection 1136793 - Interpac Technologies, Inc. - 2021-03-10](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/7cd83e8a-04e2-4611-8c87-dce997222428) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2021
- [FDA Inspection 1136793 - Interpac Technologies, Inc. - 2021-03-10](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/dd3ee3e6-2554-4144-b2b3-bd3706f55d5d) — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2021
- [FDA Inspection 697682 - Interpac Technologies, Inc. - 2010-11-09](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/23923800-d881-4467-8240-744fb5642a62) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 9, 2010
- [FDA Inspection 682394 - Interpac Technologies, Inc. - 2010-10-15](https://www.globalkeysolutions.net/records/fda_inspections/interpac-technologies-inc/b97d742b-b15e-4d0b-97f5-d06b0299e03f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 15, 2010

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