FDA Inspection 1157262 — WHITMAN LABORATORIES LTD.

WHITMAN LABORATORIES LTD. — FEI 3004347567

The FDA completed an inspection of WHITMAN LABORATORIES LTD. on May 26, 2021 in Petersfield. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 26, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Petersfield (United Kingdom)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.