FDA inspection

LiquidCapsule Manufacturing, LLC: FDA inspection ending Oct 20, 2014

FDA inspection 900467 · Official Action Indicated (OAI) · Tampa, FL

Key facts

Inspection ID 900467
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 2015
Inspection end date Oct 20, 2014
Classification Official Action Indicated (OAI)
Project area Food Composition, Standards, Labeling and Econ
Product type Food/Cosmetics
Warning letter 446062

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • Yes 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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