# R 338.555

IRI: <https://ontology.bommaritollc.com/id/01a0d9ba-7efa-7114-b786-69091d304dd1>

Type: [schema:Legislation](https://schema.org/Legislation)

- `adms:identifier`: [mi-admin-code-rule R 338.555](https://ontology.bommaritollc.com/id/01a0d9ba-7efb-7353-8899-8c86cc4cc12d)
- `prov:wasDerivedFrom`: [evidence from https://ars.apps.lara.state.mi.us/AdminCode/DownloadAdminCodeFile?FileName=R%20338.471%20to%20R%20338.592.pdf](https://ontology.bommaritollc.com/id/01a0d9ba-7eba-726a-be20-fa2203da5db4)
- `schema:isPartOf`: [Pharmacy – General Rules (R 338.471 to R 338.592)](https://ontology.bommaritollc.com/id/01a0d9ba-3d44-7698-8a6e-5beafac9329b)
- `schema:legislationIdentifier`: R 338.555
- `schema:legislationJurisdiction`: [Michigan](https://ontology.bommaritollc.com/id/01a0ca47-57ff-7219-9e2f-cdc1b39bd0fa)
- `schema:legislationLegalForce`: [schema:InForce](https://schema.org/InForce)
- `schema:legislationType`: [administrative rule](https://ontology.bommaritollc.com/vocab/leg/adminRule)
- `schema:name`: Federal regulation on good manufacturing practice for finished pharmaceuticals; adoption by reference; compliance
- `skos:prefLabel`: R 338.555

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