FDA inspection

Aerosol and Liquid Packaging, Inc.: FDA inspection ending Sep 13, 2016

FDA inspection 987788 · Voluntary Action Indicated (VAI) · Baltimore, MD

Key facts

Inspection ID 987788
Firm Aerosol and Liquid Packaging, Inc.
FEI number 1120890
Address 3701a Southwestern Blvd Ste 100
City Baltimore
State MD
ZIP 21229
Country United States
Fiscal year 2016
Inspection end date Sep 13, 2016
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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