FDA inspection

LiquidCapsule Manufacturing, LLC: FDA inspection ending Dec 7, 2021

FDA inspection 1159236 · Voluntary Action Indicated (VAI) · Tampa, FL

Key facts

Inspection ID 1159236
Firm LiquidCapsule Manufacturing, LLC
FEI number 3006676534
Address 9216 Palm River Rd Ste 203
City Tampa
State FL
ZIP 33619
Country United States
Fiscal year 2022
Inspection end date Dec 7, 2021
Classification Voluntary Action Indicated (VAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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