FDA inspection

Calmo Manufacturing, Inc: FDA inspection ending Jan 25, 2012

FDA inspection 765552 · No Action Indicated (NAI) · Huntington Beach, CA

Key facts

Inspection ID 765552
Firm Calmo Manufacturing, Inc
FEI number 3007621443
Address 16601 Burke Ln
City Huntington Beach
State CA
ZIP 92647
Country United States
Fiscal year 2012
Inspection end date Jan 25, 2012
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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