P & L Development, LLC

FDA Regulatory Profile

P & L Development, LLC appears in FDA public data with 1 recall, 0 510(k) clearances, 25 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0694-2017, Class III) was initiated on April 17, 2017.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
25
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-0694-2017Class IIIAllergy Relief Diphenhydramine HCl 25 mg, Antihistamine, Dye-Free, 24 Softgels, distributed under thApril 17, 2017