# Habp Global - Inspection Records

Source: https://www.keypedia.com/companies/habp-global/239da18a-6b35-4e8a-bbc0-416c0c8ffd8a

> Inspection records and compliance data for Habp Global in Piscataway, New Jersey. Access full analysis and detailed observations.

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## Details

- Name: Habp Global
- FEI Number: 3012017895
- City: Piscataway
- State: New Jersey
- Country Name: United States
- Address Line 1: 48 Colonial Dr
- Zip Code: 08854

## Related Documents

- [FDA Inspection 1264359 - Habp Global - 2025-03-27](https://www.keypedia.com/records/fda_inspections/habp-global/5c9dd042-9554-4bf4-b5ed-061e967aeb42) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1264359 - Habp Global - 2025-03-27](https://www.keypedia.com/records/fda_inspections/habp-global/06d4349e-65ff-46c6-b9de-a6abc4ee1c6d) — source: FDA, date: March 27, 2025
- [FDA Inspection 1264359 - Habp Global - 2025-03-27](https://www.keypedia.com/records/fda_inspections/habp-global/d8e29175-8ef0-4992-8733-15feeab6b472) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1264359 - Habp Global - 2025-03-27](https://www.keypedia.com/records/fda_inspections/habp-global/95fee7e8-d48e-4501-a5a1-05f5966dcbc4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1264359 - Habp Global - 2025-03-27](https://www.keypedia.com/records/fda_inspections/habp-global/ef80b53b-7bd1-4e02-b94d-ee8decd5ccf6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2025
- [FDA Inspection 1211209 - Habp Global - 2023-07-27](https://www.keypedia.com/records/fda_inspections/habp-global/946df9a3-a87a-4728-b81c-fed1e6cb4fc5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 27, 2023
- [FDA Inspection 1160674 - Habp Global - 2022-01-18](https://www.keypedia.com/records/fda_inspections/habp-global/ebe52cde-64a7-4c60-b57f-14e70436dc3b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 18, 2022

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