FDA inspection

Merrimack Manufacturing Llc: FDA inspection ending Jun 14, 2022

FDA inspection 1173135 · No Action Indicated (NAI) · Manchester, NH

Key facts

Inspection ID 1173135
Firm Merrimack Manufacturing Llc
FEI number 3015192982
Address 540 N Commercial St Ste 110
City Manchester
State NH
ZIP 03101
Country United States
Fiscal year 2022
Inspection end date Jun 14, 2022
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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