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.
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
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 |
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Open risk flags
- The most recent inspection outcome was VAI, on 6 November 2025.
Sources on this page
- FDA
- Drug master files, establishment registration, inspection classifications
- EDQM
- Certificates of suitability
- EudraGMDP and national regulators
- GMP certificates