Suppliers / Lloyd Inc. of Iowa

Lloyd Inc. of Iowa

United States Updated 9 July 2026

Lloyd Inc. of Iowa is a finished-dose manufacturer based in United States. It appears in 13 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 6 November 2025 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
13
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
8 of 8 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 6 November 2025 VAI US FDA
  • 15 September 2023 VAI US FDA
  • 2 February 2018 VAI US FDA
  • 28 October 2015 NAI US FDA
  • 20 February 2015 VAI US FDA
  • 16 April 2013 OAI US FDA
  • 15 June 2012 VAI US FDA
  • 9 September 2011 NAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Shenandoah, United States 1911196

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 13 None
US FDA None 1

Questions about Lloyd Inc. of Iowa

Does Lloyd Inc. of Iowa hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Lloyd Inc. of Iowa. It does have 13 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Lloyd Inc. of Iowa FDA-registered?
One site operated by Lloyd Inc. of Iowa carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Lloyd Inc. of Iowa's last inspection go?
The most recent inspection on record closed on 6 November 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 8 inspections are on file, of which 1 closed as OAI.
Where does Lloyd Inc. of Iowa manufacture?
1 registered site is on record, in United States (Shenandoah). Every site is listed on this page with the register it came from.
Which regulators recognise Lloyd Inc. of Iowa's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 6 November 2025.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates