# Maola High Point LLC, High Point, NC – FDA Inspections

Source: https://www.keypedia.com/companies/maola-high-point-llc/a371baaa-76a5-49cc-bb9d-6ef299a1c8cc

> Inspection records and compliance data for Maola High Point LLC in High Point, North Carolina. 5 FDA inspections on record, 2 Form 483s, last inspected June 25, 2025.

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## Details

- Name: Maola High Point LLC
- FEI Number: 1017599
- Address Line 1: 1900 N Main St
- City: High Point
- State: North Carolina
- Zip Code: 27262
- Country Name: United States
- Address: 1900 N Main St, High Point, North Carolina 27262, United States
- Country: United States

## Related Documents

- FDA Inspection 1275569 - Maola High Point LLC - 2025-06-25 — source: FDA, date: June 25, 2025
- FDA Inspection 1275569 - Maola High Point LLC - 2025-06-25 — source: FDA, date: June 25, 2025
- FDA Inspection 1275569 - Maola High Point LLC - 2025-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2025
- FDA Inspection 1275569 - Maola High Point LLC - 2025-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2025
- FDA Inspection 1275569 - Maola High Point LLC - 2025-06-25 — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2025
- FDA Inspection 1179901 - Maola High Point LLC - 2022-05-23 — classification: No Action Indicated (NAI), source: FDA, date: May 23, 2022
- [FDA Inspection 1069389 - Maola High Point LLC - 2018-10-22](https://www.keypedia.com/records/fda_inspections/maola-high-point-llc/e80bcbac-4835-432e-a5c4-280feeb88848) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 22, 2018
- [FDA Inspection 995094 - Maola High Point LLC - 2016-11-08](https://www.keypedia.com/records/fda_inspections/maola-high-point-llc/ac3ffd44-42e0-4caa-98b2-f35131f97bb2) — source: FDA, date: November 8, 2016
- [FDA Inspection 759156 - Maola High Point LLC - 2011-12-09](https://www.keypedia.com/records/fda_inspections/maola-high-point-llc/cf48d04f-3425-41e4-96a6-13caafbc2805) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 9, 2011

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